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