Bioness L300

Bioness L300

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



The product series includes 6 products of which 1 product is discontinued.

» Summarize specifications

Product 1 of 6
Bioness L100 GO


HMI-no.
128135

Registration date
10-02-2021
Last updated
02-03-2021

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 6
Bioness L300

The product was discontinued from Bandagist Jan Nielsen A/S 07-01-2026


HMI-no.
88198

Registration date
19-08-2015
Last updated
07-01-2026

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 
No information about CE-marking 
The supplier has not provided any information about CE-marking of the product. Explain CE-marking

Product 3 of 6
Bioness L300 GO


HMI-no.
128133

Registration date
10-02-2021
Last updated
02-03-2021

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 6
Bioness L300 GO Plus


HMI-no.
128134

Registration date
10-02-2021
Last updated
02-03-2021

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 5 of 6
Bioness L300 GO Stand-Alone


HMI-no.
128136

Registration date
10-02-2021
Last updated
02-03-2021

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 6 of 6
Bioness L300 plus


HMI-no.
109733

Registration date
22-05-2018
Last updated
02-03-2021

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 
No information about CE-marking 
The supplier has not provided any information about CE-marking of the product. Explain CE-marking