Uvod............................................................................................................................................................4

Opis proizvoda.......................................................................................................................................4

Indikacije za uporabu..............................................................................................................................4

Kliničke koristi ........................................................................................................................................4

Kontraindikacije .....................................................................................................................................4

Predviđeni rok trajanja ............................................................................................................................5

Odlaganje u otpad/recikliranje .................................................................................................................5

Specifikacije ..........................................................................................................................................5

Europska uredba REACH .......................................................................................................................6

Ilustracija proizvoda................................................................................................................................7

Podaci za kontakt...................................................................................................................................7

Serijski broj............................................................................................................................................8

Značajke madraca Isolibrium PE ....................................................................................................................9

Postavljanje................................................................................................................................................10

Tijekom rada ..............................................................................................................................................13

Postavljanje posteljine ..........................................................................................................................13

Pozicioniranje pacijenta na potporni madrac...........................................................................................13

Rješavanje inkontinencije i odvoda ........................................................................................................14

Aktiviranje kardiopulmonalne reanimacije...............................................................................................14

Resetiranje kardiopulmonalne reanimacije .............................................................................................16

Premještanje potpornog madraca..........................................................................................................17

Prijenos pacijenta s jedne platforme za potporu pacijenta na drugu ..........................................................18

Pohrana proizvoda ...............................................................................................................................18

Dodatna oprema i dijelovi ............................................................................................................................19

Održavanje donje navlake ...........................................................................................................................20

Čišćenje.....................................................................................................................................................22

Dezinfekcija................................................................................................................................................23

Preventivno održavanje ...............................................................................................................................24

Informacije o elektromagnetskoj kompatibilnosti............................................................................................26

2973-009-005 Rev AF.0