Palm Extensor Modular Pad


Classification
12 25 09 02 - Hand and elbow modules for wheelchair arm supports

Documents


The product series contains 4 products.

Product 1 of 4
Palm Extensor Modular Pad, left, large


HMI-no.
111778
Article-no.
840000100064

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
Palm Extensor Modular Pad, left, small


HMI-no.
111784
Article-no.
840000100065

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
Palm Extensor Modular Pad, right, large


HMI-no.
111781
Article-no.
840000100066

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
Palm Extensor Modular Pad, right, small


HMI-no.
111787
Article-no.
840000100067

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