Hovedstøtte til Zitzi Delfi Pro




Classification
12 25 12 01 - Head and neck supports for wheelchairs

Documents
Brochure


The product series contains 4 products.
The product series also includes 4 discontinued products. Include discontinued products.

» Summarize specifications

Product 1 of 4
Headrest for Delfi Pro


HMI-no.
105344
Article-no.
285515

Registration date
24-05-2017
Last updated
11-09-2025

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
Headrest for Delfi Pro


HMI-no.
105345
Article-no.
285518

Registration date
24-05-2017
Last updated
11-09-2025

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
Headrest for Delfi Pro


HMI-no.
86179
Article-no.
285517

Registration date
08-12-2014
Last updated
11-09-2025

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
Headrest for Delfi Pro


HMI-no.
86180
Article-no.
285516

Registration date
08-12-2014
Last updated
11-09-2025

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