LINET Sprint 100 Operating instructions

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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
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
Copyright © L I N E T, s.r.o., 2021
Translation © L I N E T, s.r.o., 2021
All rights reserved.
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
3
 .............................................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
5
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
7
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
9
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
11
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
1
1
5
5
6
6
7
7
8
8
9
9
4
4
2
2
3
3
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
13
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)
1
2
4
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
15
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
17
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
19
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
/