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Underlag, ABENA Abri-Soft Superdry
Classification
09 30 42 01 - Non-body-worn single-use products for absorbing urine and faeces
Documents
BrochureThe product series includes 4 products of which 1 product is discontinued.
Product 1 of 4
Underlag, ABENA Abri-Soft Superdry, 180x70cm, lyseblå, med flaps
The product was discontinued from Abena A/S 30-03-2023HMI-no.
107875
Article-no.
254114
Registration date
12-12-2017
Last updated
30-03-2023
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 4
Underlag, ABENA Abri-Soft Superdry, 60x40cm, lyseblå
HMI-no.
107876
Article-no.
254115
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 4
Underlag, ABENA Abri-Soft Superdry, 60x60cm, lyseblå
HMI-no.
107877
Article-no.
254119
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 4 of 4
Underlag, ABENA Abri-Soft Superdry, 90x60cm, lyseblå
HMI-no.
107878
Article-no.
254123
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