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
Classification
06 15 00 01 - Functional neuromuscular stimulators and hybrid orthoses
The product series contains 6 products.
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
HMI-no.
88198
Registration date
19-08-2015
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
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