LINET Sprint 100 Operating instructions

Brand: LINET

Model: Sprint 100

Type: Operating instructions

Sprint 100

Universal Transport Stretcher

with scales and without scales

D9U001ES1-0110

Version: 08

Publication Date: 2021-07

Instructions for Use

and Technical Description

D9U001ES1-0110_082

Manufacturer:

L I N E T spol. s r.o.

Želevčice 5

274 01 Slaný

Tel.: +420 312 576 111

Fax: +420 312 522 668

E-mail: [email protected]

http://www.linet.com

Service department: [email protected]

Sprint 100

Universal Transport Stretcher

Author: L I N E T, s.r.o.

Related links: www.linet.com

D9U001ES1-0110

Version: 08

Publication Date: 2021-07

Translation © L I N E T, s.r.o., 2021

All trademarks and brands are the property of the appropriate owners. The manufacturer reserves the right to changes in the

contents of the instructions for use that relate to the product´s technical regulations. It is for this reason that the contents of the in-

structions for use may indicate dierences from the current manufacture of the product. Reproduction, also excerpts, only with prior

permission of the publisher. Subject to changes due to technical developments. All technical data are rated data and are subject to

construction and manufacturing tolerances.

D9U001ES1-0110_08

 .............................................4

1.1 Warning Notices .......................................................... 4

1.1.1 Types of Warning Notices ........................................4

1.1.2 Structure of Warning Notices ...................................4

1.2 Instructions ..................................................................4

1.3 Lists .............................................................................4

1.4 Symbols on the Package ............................................5

1.5 Symbols on the Bed .................................................... 6

1.6 Symbols on the Mattress ............................................9

1.7 Serial Label with UDI ..................................................11

1.7.1 Sprint 100 without scales .........................................11

1.7.2 Sprint 100 with scales ..............................................11

1.7.3 Serial Label with UDI (Sprint 100) ............................12

1.7.4 Serial Label with UDI (mattress) ..............................13

1.7.5 Serial Label (accessory) ..........................................14

1.8 Acoustic signalisation (only Sprint 100 with scales) .... 15

1.9 Denitions ...................................................................15

1.10 Abbreviations ............................................................16

2 Safety Instructions .......................................................17

3 Intended use (Sprint 100 without scales) ..................19

3.1 User population ........................................................... 19

3.2 Contraindications ........................................................19

3.3 Operator ...................................................................... 19

4 Intended use (Sprint 100 with scales) ........................ 20

4.1 User population ........................................................... 20

4.2 Contraindications ........................................................20

4.3 Operator ...................................................................... 20

5 Intended use (Sprint 100 mattresses) ........................20

5.1 User population ........................................................... 20

5.2 Contraindications ........................................................20

5.3 Operator ...................................................................... 20

6 Product Description ..................................................... 21

6.1 Hierarchy of Product Variants ..................................... 21

6.2 SPRINT 100 WITH 4-PART MATTRESS SUPPORT PLAT-

FORM ............................................................................... 22

6.3 SPRINT 100 WITH 2-PART MATTRESS SUPPORT PLAT-

FORM ............................................................................... 23

 ...............................................24

7.1 Identication of Applied Parts (Type B) ....................... 24

7.2 Mechanical Specications (Sprint 100) ....................... 24

7.2.1 Sprint 100 with Standard Mattress Support Platform

..........................................................................................24

7.2.2 Sprint 100 with Wide Mattress Support Platform .....25

7.3 Electrical Specications (only Sprint 100 with scales) 26

7.4 Environment Conditions (Sprint 100) ..........................26

7.5 Electromagnetic Compatibility (only Sprint 100 with scales)

..........................................................................................27

7.5.1 Manufacturer instructions - electromagnetic emissions

..........................................................................................27

7.5.2 Manufacturer instructions - electromagnetic susceptibility

..........................................................................................28

8 Use and Storage Conditions ....................................... 29

9 Scope of Delivery and Product Variants .................... 30

9.1 Delivery .......................................................................30

9.2 Scope of Delivery ........................................................ 30

9.3 Sprint 100 Variants ......................................................30

10 Putting into Service ...................................................31

10.1 Mattress Support Platform ........................................32

10.2 Potential Interconnection (optional) ..........................33

10.3 Before Use ................................................................33

10.4 Transport ................................................................... 33

10.5 Firmware ...................................................................34

11 Adaptor and Power Supply Cord (only Sprint 100 with

scales) .............................................................................34

11.1 Connection of the Power Supply Cord to the Adaptor

..........................................................................................35

11.2 Indication of the bed connected to the mains ............ 40

12 Batteries (only Sprint 100 with scales) ....................41

12.1 Battery Activation ......................................................42

12.2 Battery Capacity Status Indicators ............................ 43

12.3 Pop-up windows connected with Battery Capacity Status

..........................................................................................43

12.4 Change of the 4 batteries in Battery Box ..................44

13 Manipulation ............................................................... 46

13.1 Collapsible Siderails ..................................................47

13.2 Castor Control ........................................................... 48

13.2.1 Braked Bed ............................................................49

13.2.2 Forward Movement (Steering) ...............................49

13.2.3 Unrestricted Movement .......................................... 50

13.3 Bed Positioning .........................................................51

13.3.1 Backrest .................................................................51

13.3.2 Thighrest (only 4-part Mattress Support Platform) . 52

13.3.3 Calfrest (only 4-part Mattress Support Platform) ...53

13.3.4 Lifting ....................................................................54

13.3.5 Lowering ...............................................................55

13.3.6 Trendelenburg Position ..........................................56

13.3.7 Anti-Trendelenburg Tilt ...........................................57

13.3.8 Cardiac Chair Position (only 4-part Mattress Support Plat-

form) .................................................................................58

13.4 CPR Backrest Release .............................................59

13.4.1 The 2-part Mattress Support Platform .................... 59

13.4.2 The 4-part Mattress Support Platform .................... 60

14 Scales Control (only Sprint 100 with scales) ..........61

14.1 Preparation ...............................................................61

14.2 Displaying .................................................................61

14.3 Zeroing ...................................................................... 62

14.4 Bed Overload ............................................................63

14.5 Bed Underload ..........................................................63

14.6 Weighing in tilt ........................................................... 63

14.7 Calibration of the Zero ..............................................63

14.8 Pop-up windows connected with Scales Control ......64

15 Bed Exit Alarm Monitoring (only Sprint 100 with scales)

..........................................................................................64

15.1 Preparation ...............................................................65

15.2 Displaying .................................................................65

15.3 Activation ...................................................................66

15.4 Monitored Zone ......................................................... 66

15.5 PAUSE ......................................................................66

15.6 BED EXIT ALARM .....................................................67

15.7 Deactivation ..............................................................67

15.8 Pop-up windows connected with Bed Exit Alarm Monitoring

..........................................................................................68

16 Equipment ..................................................................69

16.1 Accessory Holders ....................................................69

16.2 Accessory Rail with plastic hooks .............................70

16.3 DIN Rail .....................................................................71

16.4 Undercarriage Cover .................................................72

16.5 FlexiDrive (Sprung Retractable Fifth Castor) ............72

16.6 IV&Drive (Infusion Stands/Pushing Handles) ...........73

16.7 Handles ..................................................................... 74

16.7.1 Removable handles ...............................................74

16.7.2 Foldable handles ....................................................75

16.7.3 Fixed handles .........................................................76

16.8 Angle Indicators (optional) ........................................76

16.9 Examination with C-arm (in-bed uoroscopy) ...........77

17 Mattress ......................................................................78

17.1 Anti-slip coating ......................................................... 79

17.2 Installation of Passive Mattress ................................79

17.2.1 Straps with side release buckles ............................79

17.3 Mattresses Specications .........................................81

17.3.1 Sprint 100 with Standard Mattress Support Platform

..........................................................................................81

17.3.2 Sprint 100 with Wide Mattress Support Platform ...82

17.4 Cleaning of Passive Mattress ...................................83

Table of Contents

D9U001ES1-0110_084

1 

1.1 Warning Notices

1.1.1 Types of Warning Notices



► CAUTION warns about the risk of material damage.

► WARNING warns about the risk of physical injury.

► DANGER warns about the risk of fatal injury.

1.1.2 Structure of Warning Notices

SIGNAL WORDS!

Type and source of danger!

► Measures to avoid the danger.

1.2 Instructions

Structure of instructions:

► Perform this step.

Results, if necessary.

1.3 Lists

Structure of bulleted lists:

 List level 1

 List level 2

List level 3

17.4.1 General Guidance .................................................. 83

17.4.2 Routine Cleaning and Disinfection ......................... 84

17.4.3 Complete Cleaning and Disinfection ...................... 84

17.4.4 Mattress Core ........................................................84

18 Accessories ................................................................85

18.1 Infusion Stand ...........................................................86

18.2 Telescopic Infusion Stand .........................................87

18.3 Chart Holder ..............................................................87

18.4 Monitor Shelf ............................................................. 88

18.5 Paper Roll Holder ......................................................89

18.6 Storage Space ..........................................................90

18.7 Oxygen Bottle Holder ................................................ 91

18.8 X-Ray Cassette Holder .............................................92

18.8.1 Instructions for X-Ray Examination ........................97

19 Cleaning/Disinfection ................................................99

19.1 Cleaning (Sprint 100) ................................................101

19.1.1 Cleaning before Changing Patients .......................101

19.1.2 Daily Cleaning ........................................................ 101

19.1.3 Complete Cleaning and Disinfection ...................... 102

20 Troubleshooting (Sprint 100 without scales) ..........102

21 Troubleshooting (Sprint 100 with scales) ................ 103

21.1 Fault Codes ...............................................................103

21.2 Pop-up windows ........................................................104

22 Maintenance (Sprint 100 without scales) .................106

22.1 Regular maintenance ................................................ 106

22.2 Spare Parts ...............................................................106

22.3 Safety Technical Checks ........................................... 106

23 Maintenance (Sprint 100 with scales) ......................107

23.1 Regular maintenance ................................................ 107

23.2 Spare Parts ...............................................................107

23.3 Safety Technical Checks ........................................... 107

24 Disposal (Sprint 100 without scales) .......................108

24.1 Environment Protection .............................................108

24.2 Disposal ....................................................................108

24.2.1 Within Europe ........................................................108

24.2.2 Outside Europe ......................................................108

25 Disposal (Sprint 100 with scales) .............................109

25.1 Environment Protection .............................................109

25.2 Disposal ....................................................................109

25.2.1 Within Europe ........................................................109

25.2.2 Outside Europe ......................................................109

26 Warranty ......................................................................110

27 Standards and Regulations ......................................110

27.1 Sprint 100 ..................................................................110

27.2 Manufacturer ............................................................. 110

D9U001ES1-0110_08

1.4 

FRAGILE, HANDLE WITH CARE

THIS WAY UP

KEEP DRY (PROTECT FROM HUMIDITY)

PAPER RECYCLING SYMBOL

DO NOT USE HAND TRUCK HERE

DO NOT STACK DURING STORAGE

D9U001ES1-0110_086

1.5 Symbols on the Bed

READ INSTRUCTIONS FOR USE

SAFE WORKING LOAD

WARNING AGAINST CRUSHING OR TRAPPING

JACK FOR ATTACHMENT OF CONDUCTOR FOR POTENTIAL

EQUALISATION

WARNING

APPLIED PARTS TYPE B

ONLY SUITABLE FOR INDOOR USE

MAXIMUM WEIGHT OF PATIENT

WEIGHT OF BED (depending on con guration)

MET MARK

RECYCLING SYMBOLS

DO NOT POLLUTE THE ENVIRONMENT

D9U001ES1-0110_08

MAXIMUM LOAD OF THE MONITOR SHELF 15 KG

PLACE MONITOR ON THIS SIDE OF THE MONITOR SHELF

MAXIMUM LOAD OF THE MONITOR SHELF 15 KG

DO NOT PLACE MONITOR ON THIS SIDE OF THE MONITOR SHELF

INSTRUCTION FOR PLACEMENT OF THE MONITOR SHELF

(L=LEFT, R=RIGHT)

MAXIMUM LOAD OF ONE HOOK 5 KG

FOLD THE MARKED FOLDABLE INFUSION STAND AS THE FIRST ONE

MAXIMUM LOAD OF ONE HOOK 5 KG

FOLD THE MARKED FOLDABLE INFUSION STAND AS THE SECOND ONE

MANUFACTURER

MANUFACTURING DATE

REFERENCE NUMBER

(PRODUCT TYPE DEPENDING ON CONFIGURATION)

SERIAL NUMBER

D9U001ES1-0110_088

MEDICAL DEVICE (COMPATIBLE WITH MEDICAL DEVICE REGULATION)

WEEE SYMBOL (RECYCLE AS ELECTRONIC WASTE,

DO NOT PUT INTO THE HOUSEHOLD WASTE)

BATCH NUMBER (ACCESSORIES)

UNIQUE DEVICE IDENTIFICATION (FOR MEDICAL DEVICES)

MASS OF MOBILE HOSPITAL BED (MASS OF EMPTY BED + SAFE WOR-

KING LOAD)

DOUBLE INSULATION SYMBOL, DEVICE OF THE PROTECTION CLASS II

(CLASSIFIED ACCORDING TO THE TYPE OF PROTECTION FROM ELECT-

RIC SHOCK, ONLY FOR Sprint 100 WITH SCALES)

Fig. Warning, read

instructions for use

Fig. Example of Scales LW20 label (only Sprint 100 with scales)

D9U001ES1-0110_08

READ INSTRUCTIONS FOR USE

CE MARKING (PRODUCT NORMATIVELY HARMONIZED FOR EUROPEAN

ECONOMIC AREA)

COVER MATERIALS ARE FIRE RESISTANT

TO BS7175, SOURCE 0, 1 AND 5

DO NOT IRON

DO NOT USE PHENOL

DO NOT WRING

REGULARLY INSPECT THE INSIDE OF THE COVER FOR CONTAMINATION

MACHINE WASH AT MAX. 71°C FOR 3 MINUTES

DISINFECT USING SOLUTION CONTAINING LESS THAN 1000 ppm OF

CHLORINE (REFER TO INSTRUCTIONS FOR USE)

RINSE WITH WATER

1.6 Symbols on the Mattress

D9U001ES1-0110_0810

TUMBLE DRY ON LOW HEAT SETTING (MAX. 60°C)

MATTRESS FOOT PART

HANDWASH WITH DETERGENT (INITIAL TEMPERATURE OF HOT WATER

SHOULD NOT EXCEED 50°C)

Fig. Label with applied patents

D9U001ES1-0110_08

1.7 Serial Label with UDI

Fig. Position of serial label on the bed (Sprint 100 without scales)

Fig. Position of serial label on the bed (Sprint 100 with scales)

1.7.1 Sprint 100 without scales

There is a serial label of the bed under the Backrest.

1.7.2 Sprint 100 with scales

There is a serial label of the bed with scales on the left side of the frame of the mattress support platform next to the Backrest.

D9U001ES1-0110_0812

Fig. Serial Label with UDI (Sprint 100 without scales)

Fig. Serial Label with UDI (Sprint 100 with scales)

1ES15308-190 (Sprint 100 without scales)

REF

SN ORDER:

20200130108 20007711

2021-02-12

(01) 8592654232903

(11) 210212

(21) 20200130108

N/A

CUC:

UDI

1ES115409-5 (Sprint 100 with scales)

REF

SN ORDER:

20210173945 20019930

2021-05-19

(01) 8592654275801

(11) 210519

(21) 20210173945

N/A

CUC:

UDI

1Address of Manufacturer

2Manufacturing Date (Year-Month-Day)

3DI (Device Identier) / GTIN (Global Trade Item Number)

41D Bar code GS1-128 (Serial Number)

5Symbols

6 Conguration number

7 Serial Number

8PI (Product Identier)

92D Bar Code (GS1 DataMatrix) DI+PI=UDI

1.7.3 Serial Label with UDI (Sprint 100)

Pictures of serial labels below serve just for explanation of the signs and elds on the serial labels.

D9U001ES1-0110_08

4GPTK17000S 4GPUL17000S

193x76x13 cm

4GPVM17000S

4GPVU1700AS

193x76x13 cm

4GPVU17000S

30 x 76 x 5"

S100W2-30765

550 lbs.

S100W4-30765

30 x 76 x 5"

193x76x13 cm

4GPVU1700AS

30 x 76 x 5"

S100W4-30765

550 lbs.

S100W4-30765

30 x 76 x 5"

Fig. Mattress Label

(Sprint Standard

for Sprint 100 with

Standard Mattress

Support Platform)

Fig. Mattress Label

(Sprint Comfort

for Sprint 100 with

Standard Mattress

Support Platform)

Fig. Mattress Label

(Sprint Advanced

for Sprint 100 with

Standard Mattress

Support Platform)

Fig. Mattress Label

(Sprint Advanced for

Sprint 100 with Wide

Mattress Support

Platform - version 1)

Fig. Mattress Label

(Sprint Advanced

for Sprint 100 with

2-part Wide Mattress

Support Platform -

version 2)

Fig. Mattress Label

(Sprint Advanced

for Sprint 100 with

4-part Wide Mattress

Support Platform -

version 3)

1.7.4 Serial Label with UDI (mattress)

D9U001ES1-0110_0814

1Address of Manufacturer

2Manufacturing Date (Year-Month-Day)

41D Bar code GS1-128 (Serial Number)

Fig. Accessory Label

11011410A0000

REF

LOT 100047121

2021-03-09

11011410A0000

REF

LOT 100047121

2021-03-09

1.7.5 Serial Label (accessory)

Picture of serial label below serve just for explanation of the signs and elds on the serial label.

D9U001ES1-0110_08

1.8 Acoustic signalisation (only Sprint 100 with scales)

SOUND MEANING

REPEATED MELODY: beep, pause, beep, pause,

beep, longer pause

Bed Exit Alarm

 Conrmation of the successfully activated Bed Exit Alarm Monitoring

BEEP lasting 0,2s Conrmation of Stabilized Scales during Zeroing

3 BEEPS: 0,125s sound / 0,125s silence Notication

1.9 

 the pricelist model conguration, not including a mattress

Bed Weight The value depends on the product conguration, accessories or

customer adjustments.

Clearance of Undercarriage the height from the oor to the lowest point of the undercarriage

between the castors, for the manipulation of accessories under a

braked bed in the standard position

Reference number Reference number depends on conguration.

 the highest allowable load on the bed (patient, mattress, accesso-

ries and the load supported by those accessories)

Siderail Height the height of the upper crossbar or the edges of the siderails (not

the highest point of the siderail controls) from the patient surface

Standard Bed Position - The height of the mattress support platform with regard to the

oor is 56,5 cm (2-part Mattress Support Platform) or 55,5 cm (4-

part Mattress Support Platform)

- The Mattress Support Platform, including the individual parts, has

to be in a horizontal (level - 0°) position.

- The siderails are always locked in the upper position.

Adult Patient having a physical size equal to or more than 146 cm, a

mass equal to or more than 40 kg and a body mass index (BMI)

equal to or more than 17 (according to IEC 60601-2-52).

Mass of mobile hospital bed Sum of empty bed mass and Safe Working Load.

D9U001ES1-0110_0816

AC ( ~ ) Alternating Current

BEA Bed Exit Alarm Monitoring

CPR Cardiopulmonary Resuscitation

dBA Sound Intensity Unit

DC ( ) Direct Current

CUC Conguration number

EMC Electromagnetic Compatibility

HF High Frequency

HPL High Pressure Laminate

IP Ingress Protection

IV Intravenous

LED Light Emitting Diodes

ME Medical Electrical (Equipment)

MET MET Laboratories testing and certifying for the U.S. market

ON Activation

OFF Deactivation

ppm parts per million, millionth (1000 ppm = 0,1%)

REF Reference Number (product type depending on conguration)

SN Serial Number

SWL Safe Working Load

UDI Unique Device Identication (for medical devices)

WEEE Waste from Electrical and Electronic Equipment

1.10 Abbreviations

D9U001ES1-0110_08

WARNING!



mechanical damages is hazardous!

2 Safety Instructions

WARNING!

Any serious incident that has occurred in relation to the device should be reported to the manufacturer and the

competent authority of the Member State in which the user and/or patient is established!

WARNING!

This medical device is not intended for oxygen enriched environment!

WARNING!



WARNING!

This medical device is not portable medical electrical equipment!

WARNING!

Patient is allowed to use selected control elements only if hospital personnel had assessed that the patient´s

physical and psychological state is in accordance with use of them and only if the hospital personnel had

trained the patient in accordance with the instructions for use!

WARNING!



WARNING!

-

ble for spinal cord injuries! Trendelenburg position is not suitable for patients with higher intracranial pressu-

re!

WARNING!



support platform!

WARNING!

Hospital personnel is allowed to use the weighing system (scales) for weighing patients only if they had been

trained according to the instructions for use!

WARNING!

Only authorised and trained personnel equipped with an appropriate tool are allowed to change fuse in Battery

Box!

WARNING!



of Sprint 100 with scales.

WARNING!



100 with scales ME equipment may occur.

D9U001ES1-0110_0818

Additional Instructions for correct use:

► Follow the instructions for use carefully.

► Use the bed exclusively if it is in perfect working order.

► If necessary, check the bed functions daily or at each shift change.

► Ensure any user has read and understood this manual completely before operating the product.

► Ensure that the bed is operated exclusively by qualied personnel who have been trained according to the instructions for

use.

► Ensure that the patient (health permitting) has been informed about the operation of the bed and all applicable safety

instructions.

► Move the bed exclusively on even, hard-surfaced oors.

► Replace any damaged parts immediately with original spare parts.

► Ensure that maintenance and installation are performed exclusively by qualied personnel who have been trained by the

manufacturer.

► Before peak loads or unavoidable excess loads (CPR), place Mattress Support Platform in the lowest position.

► Ensure that only one adult patient uses the bed at any time.

► Take care to avoid injuries or squeezing when operating moving parts.

► When using lifting poles or infusion stands, ensure that nothing will be damaged when you move or adjust the bed.

► Brake the castors when the bed is occupied.

► Keep the Mattress Support Platform in the lowest position when the patient is unattended by healthcare personnel in order

to minimize risk of patient falls.

► Ensure that Siderails are operated exclusively by healthcare personnel.

► Never use the bed in areas where there is a hazard of explosion.

► Ensure that parts of the bed intended for movement are not blocked.

► To prevent failures, use exclusively the manufacturer’s original accessories and mattresses.

► Ensure that the stipulated safe working load is not exceeded.

► If the patient‘s condition could lead to an entrapment, leave the mattress support platform in the at position whilst una-

ttended.

► Adjust bed height when transporting the bed in order to facilitate overcoming possible obstacles.

► Do not modify bed and its components without the manufacturer´s approval.

► Use the mattress system exclusively as specied in this manual and in perfect working order.

► Use the mattress system exclusively in its original state and do not modify it in any way.

► Have the mattress system used exclusively by or under supervision of trained and qualied nursing personnel.

► Have the mattress system serviced and installed exclusively by qualied personnel trained and authorised by the manu-

facturer.

► Do not exceed the maximum patient weight limit (see Mechanical Specications).

► Do not use the bed in the case its parts have been removed unless these parts are designed to be removed.

► To avoid injury or crushing, take extra caution when operating any moving parts of the bed.

► When using infusion stands, ensure that nothing will be damaged when you move or adjust the bed.

► Hydraulic units and gas springs cointain an mineral oil. The mineral oil should not get into the sewerage because of toxici-

ty for water organisms.

D9U001ES1-0110_08

3 Intended use (Sprint 100 without scales)

The intended use is the short term hospitalization of the patient in the emergency departments and one day care de-

partments, or other applicable departments, which includes above all the following aspects:

► Patient transport in the stretcher in the indoor environment. For the outdoor environment specic precautions in the in-

structions for use are valid.

► Adjustment of the positions needed for the, examinations, treatments, physiotherapy, sleeping, relaxation, preventive and

mobilization reasons, routine nursing. These positions are further specied and described in the clinical evaluation of this device,

together with their potential clinical outcomes and benets.

► Providing the safe environment for the patient during all relevant procedures. The particular requirements on patient safety

are the subject of the clinical evaluation, including evaluation of the risk/benet ratio. The relevant safety issues are the part of the

risk management le.

► Providing the suitable working conditions for the caregivers to perform the routine and specic tasks during the patient

hospitalization.

3.1 User population

► Adult patients (weight >= 40 kg, height >= 146 cm, BMI >= 17) in the emergency and one day care units (Application Envi-

ronment 1, 2 and 5 as in IEC 60601-2-52)

► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)

3.2 Contraindications

► The medical device is not intended for the pediatric patients use.

► The medical device is not intended for the use with patients exceeding the Maximum Patient Weight and whose body

constitution is disproportionate to the size of Mattress Support Platform.

► The medical device is not intended for the long-term hospitalization with respect to dimensional parameters of the device

and the used mattress.

► Certain positions are not suitable for specic diagnoses/medical conditions (e.g. spinal cord injuries vs. Fowler position,

higher ICP patients vs. Trendelenburg). Sta expert assessment / nursing consideration is needed in all individual case of contrain-

dication.

3.3 Operator

► Caregiver

► Patient (based on individual patient status assessment by caregiver the patient can utilize dedicated device functions)

D9U001ES1-0110_0820

4 Intended use (Sprint 100 with scales)

The intended use is the short term hospitalization of the patient in the emergency departments and one day care de-

partments, or other applicable departments, which includes above all the following aspects:

► Patient transport in the stretcher in the indoor environment. For the outdoor environment specic precautions in the in-

structions for use are valid.

► Adjustment of the positions needed for the, examinations, treatments, physiotherapy, sleeping, relaxation, preventive and

mobilization reasons, routine nursing. These positions are further specied and described in the clinical evaluation of this device,

together with their potential clinical outcomes and benets.

► Providing the safe environment for the patient during all relevant procedures. The particular requirements on patient safety

are the subject of the clinical evaluation, including evaluation of the risk/benet ratio. The relevant safety issues are the part of the

risk management le.

► Providing the suitable working conditions for the caregivers to perform the routine and specic tasks during the patient

hospitalization.

► Indicative measurement of the patient weight, used as supportive feature without direct diagnostic eect. It helps sta to

assess the general patient status and apply the nutrition and medications.

4.1 User population

► Adult patients (weight >= 40 kg, height >= 146 cm, BMI >= 17) in the emergency and one day care units (Application Envi-

ronment 1, 2 and 5 as in IEC 60601-2-52)

► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)

4.2 Contraindications

► The medical device is not intended for the pediatric patients use.

► The medical device is not intended for the use with patients exceeding the Maximum Patient Weight and whose body

constitution is disproportionate to the size of Mattress Support Platform.

► The medical device is not intended for the long-term hospitalization with respect to dimensional parameters of the device

and the used mattress.

► Certain positions are not suitable for specic diagnoses/medical conditions (e.g. spinal cord injuries vs. Fowler position,

higher ICP patients vs. Trendelenburg). Sta expert assessment / nursing consideration is needed in all individual case of contrain-

dication.

4.3 Operator

► Caregiver

► Patient (based on individual patient status assessment by caregiver the patient can utilize dedicated device functions)

5 Intended use (Sprint 100 mattresses)

The intended use is to provide basic support surface for patient being treated on LINET’s Sprint range of stretchers only. They are

designed to provide comfort during short term use. The use of these mattresses does not remove the need for regular repositioning

in line with best clinical practice (ref: NPUAP, EPUAP).

5.1 User population

► Adult patients (weight >= 40 kg, height >= 146 cm, BMI >= 17) in the emergency and one day care units (Application Envi-

ronment 1, 2 and 5, as in IEC 60601-2-52)

► Caregivers (nurses, doctors, technical personnel, transport personnel, cleaning personnel)

5.2 Contraindications

► patient with higher risk of pressure ulcers

► patients with higher weight than mattress weight limit

► patient’s showing signs of pressure related tissue damage should be transfered onto an alternative support surface based

on risk assessment, clinical reasoning and best clinical practice (EPUAP, NPUAP guidelines)

5.3 Operator

► Caregiver

Page is loading ...

LINET Sprint 100 Operating instructions

Brand: LINET

Model: Sprint 100

Type: Operating instructions

Download PDF

report

LINET Sprint 100 Operating instructions

LINET Sprint 100 Operating instructions

Related papers

Other documents