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Underlag, ABENA Abri-Soft
Classification
09 30 42 01 - Non-body-worn single-use products for absorbing urine and faeces
Documents
BrochureThe 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 
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 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
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 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
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 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
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