All product information is provided by the supplier. The National Board of Social Services is not responsible for either contents, origin, flaws and deficiencies, or any kind of damage that may occur from the use of the information. The National Board of Social Services has no authority to endorse products and does not assess the quality of the products. Hide this message.
Stiklagen, ABENA Abri-Bed
Classification
09 30 42 01 - Non-body-worn single-use products for absorbing urine and faeces
Documents
BrochureThe product series contains 3 products.
The product series also includes a discontinued product. Include discontinued products.
Product 1 of 3
Stiklagen, ABENA Abri-Bed Regular, 2-lags, 140x80cm, lyseblå
HMI-no.
107865
Article-no.
246610
Registration date
12-12-2017
Last updated
23-08-2022
Test information
No information about tests according to standards 
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
EU product safety regulation
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device
Product 2 of 3
Stiklagen, ABENA Abri-Bed Regular, 2-lags, 175x80cm, lyseblå
HMI-no.
107866
Article-no.
246611
Registration date
12-12-2017
Last updated
23-08-2022
Test information
No information about tests according to standards
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
EU product safety regulation
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device
Product 3 of 3
Stiklagen, ABENA Abri-Bed Regular, 2-lags, 210x80cm, lyseblå
HMI-no.
107867
Article-no.
246612
Registration date
12-12-2017
Last updated
23-08-2022
Test information
No information about tests according to standards
The supplier has not provided documentation, that this product is testet according to a relevant standard. See examples of relevant standards for this product type
EU product safety regulation
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device