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Elevating Swivel Unit for Channel Forearm Pads
Classification
12 25 09 02 - Hand and elbow modules for wheelchair arm supports
Documents
BrochureThe product series contains 4 products.
Product 1 of 4
Elevating Swivel Unit for Channel Forearm Pads, Ø19
HMI-no.
111810
Article-no.
840000100077
Registration date
22-10-2018
Last updated
13-12-2024
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
Elevating Swivel Unit for Channel Forearm Pads, Ø20
HMI-no.
111811
Article-no.
840000100078
Registration date
22-10-2018
Last updated
13-12-2024
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
Elevating Swivel Unit for Channel Forearm Pads, Ø22,2
HMI-no.
111812
Article-no.
840000100079
Registration date
22-10-2018
Last updated
13-12-2024
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
Elevating Swivel Unit for Channel Forearm Pads, Ø25,4
HMI-no.
111813
Article-no.
840000100080
Registration date
22-10-2018
Last updated
17-12-2024
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