Underlag, ABENA Abri-Soft Superdry




Classification
09 30 42 01 - Non-body-worn single-use products for absorbing urine and faeces

Documents
Brochure


The product series includes 4 products of which 1 product is discontinued.

» Summarize specifications

Product 1 of 4
Underlag, ABENA Abri-Soft Superdry, 180x70cm, lyseblå, med flaps

The product was discontinued from Abena A/S 30-03-2023


HMI-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