www.humancaregroup.com 13
ENGLISH
Human Care is an ISO 13485:2016 cered
Swedish medical device company. The Quality
Management System is in compliance with US
21 CFR part 820.
The product is CE marked in accordance with EU
Direcve 93/42/EEC (MDD) and/or EU Regula-
on 2017/745 (MDR), as class I medical device.
The CE mark is on the product.
This product has been tested in accordance
with ISO 11199-2:2005.
Compliances and Standards
About our products
On delivery
Checkthefollowingbeforeusingyournew
product:
1. Check that no damage has occurred during
transport(ifthisisthecase,pleaseimmedia-
telyinformthedeliveryagent).
2. Checkthatthenumberandtype(s)of
productsdetailedonthedeliverycercate
agreewiththegoodsdelivered.
3. Check that the delivery is of the desired
modelandtypeofproduct.
Pleasecontactusimmediatelyincaseofany
deliveryproblem.
Return or refund
If any product has to be returned for any rea-
son,pleasecontactustoobtainaclaimnumber
andadviceonhowtoproceed.
The goods should be returned in complete and
undamagedcondionintheiroriginalpacka-
ging.
Thefollowinginformaonshouldaccompany
anyproductonitsreturn.Theproduct’siden-
caonnumber,deliverydate,thedatetheuser
tookpossessionoftheaid,thedateofthepro-
duct’slastservice,thepersonwhomweshould
contactaboutthefault,whetheritbetheuser
oranother,andthenatureofthefault.
Human Care HC AB reserves the right to inspect
thereturnedproduct.Ifnofaultcanbefound,
theitemwillbereturnedtotheuser.Transport
costsmaythenbechargeable.
Product lifeme
Theproduct´sexpectedlifemeisseven(7)
years,iftheproductisusedasintendedand
maintained according to the manufacturer´s
instrucons,dependingontheintensityofuse
andmaximumloadappliedduringuse.Ifthe
productlabelisnolongerlegible,theproduct
shouldbediscarded.