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SAFE Med trykaflastende Helmadras nr.201YP,GUL-ROSA, brug op til 180kg
SAFE Med pressure relieving Mattress no. 201YP molds to the body for efficient pressure distribution and stability to prevent pressure sores and promote healing. The visco-elastic SAFE foam ensures a comfortable body temperature.
Incontinence cover is breathable and stretchable with covered zipper on three sides.
Choose 12 or 14 cm high mattress
Incontinence cover is breathable and stretchable with covered zipper on three sides.
Choose 12 or 14 cm high mattress
Classification
04 33 06 13 - Foam mattresses, synthetic (PUR)
The product series contains 6 products. The product below meets the specified details.
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SAFE Med trykaflastende Helmadras nr.201YP,GUL-ROSA, 200 x 90 x 12 cm
HMI-no.
81410
Article-no.
201YP.2
Registration date
23-10-2013
Last updated
21-11-2023
Properties
Intended for children
No
Products for children must comply with the specific demands for safety as stated in certain standards. It is the supplier of the product who has stated that the product is intended for children. The National Board of Social Services holds no responsibility in relation to this assessment.
HR PUR foam
Yes
High Resilience Polyurethane foam
CM HR PUR foam
No
Combustion Modified High Resilience foam
Viscoelastic PUR foam
Yes
Temperature sensitive polyurethane foam
Intended for use with adjustable mattress support platform
Yes
Measures
Length
200
cm
For mattress extension: measure of the elongation of the mattress.
Width
90
cm
For mattress extension: equivalent to the widht of the mattress.
Height
12
cm
Mattress weight
14
kg
User weight, max
130
kg
Test information ![info](/en/img/i.svg)
Though the product is testet, it might not have passed all requirements in the standard. Besides, some products are only tested according to parts of the standard. Read the test report for detailed information. See also other standards that could be relevant for this product type.
: Tested according to other national or international standard.
Test lab: Swerea IVF AB. Test date: 07-11-2018
Test report for HMI-no. 81410
Test lab: Swerea IVF AB. Test date: 07-11-2018
EU product safety regulation ![info](/en/img/i.svg)
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device