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Sigvaris Gummihandsker
Classification
09 09 03 06 - Applying gloves
Documents
The product series contains 4 products.
The product series also includes a discontinued product. Include discontinued products.
Product 1 of 4
Sigvaris Gummihandsker, str. Large
HMI-no.
Article-no.
4404102
Registration date
15-04-2013
Last updated
21-11-2023
Properties
Size
Large
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
Sigvaris Gummihandsker, str. Medium
HMI-no.
Article-no.
4404101
Registration date
22-07-2002
Last updated
21-11-2023
Properties
Size
Medium
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
Sigvaris Gummihandsker, str. Small
HMI-no.
Article-no.
4404100
Registration date
22-07-2002
Last updated
21-11-2023
Properties
Size
Small
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
Sigvaris Gummihandsker, str. X-Large
HMI-no.
Article-no.
4404099
Registration date
22-07-2002
Last updated
21-11-2023
Properties
Size
X-Large
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