All product information is provided by the supplier. The National Board of Social Services is not responsible for either contents, origin, flaws and deficiencies, or any kind of damage that may occur from the use of the information. The National Board of Social Services has no authority to endorse products and does not assess the quality of the products. Hide this message.

Bioness L300 GO PLUS


Classification
06 15 00 01 - Functional neuromuscular stimulators and hybrid orthoses



The product series contains 1 product.

Product 1 of 1
Bioness L300 GO PLUS


HMI-no.
138715

Registration date
09-10-2023
Last updated
09-10-2023

Test information
No information about tests according to standards info
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 info
The supplier has provided the following information about CE-marking of the product. Explain CE-marking
CE marked as medical device