Underlag, ABENA Abri-Soft


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

Documents


The product series contains 4 products.

Product 1 of 4
Underlag, ABENA Abri-Soft Classic, 60x60cm, lyseblå


HMI-no.
Article-no.
4119

Registration date
12-12-2017
Last updated
23-08-2022

Test information
No information about tests according to standards info
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 info
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 Classic, 75x60cm, lyseblå


HMI-no.
107862
Article-no.
4122

Registration date
12-12-2017
Last updated
23-08-2022

Test information
No information about tests according to standards info
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 info
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 Classic, 90x60cm, lyseblå


HMI-no.
107863
Article-no.
4123

Registration date
12-12-2017
Last updated
23-08-2022

Test information
No information about tests according to standards info
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 info
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 Excellent, 90x60cm, lyseblå


HMI-no.
Article-no.
4109

Registration date
12-12-2017
Last updated
23-08-2022

Test information
No information about tests according to standards info
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 info
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device