Otto Bock Healthcare Products GmbH
AT-MF-000002920 · Austria · Wien
Otto Bock Healthcare Products GmbH is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: 8E500.
Among these devices, 6 are declared active.
Devices declared under this manufacturer
- Michelangelo Hand
- Michelangelo Hand (Service/Test)
- Michelangelo Hand - Service,Test
Catalogue references include 8E500=L-M, 8E500=L-M-OB, 8E500=L-M-S, 8E500=R-M, 8E500=R-M-OB, 8E500=R-M-S.
European nomenclature codes declared: Y061899.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Otto Bock Healthcare Products GmbH (AT) · FDA 3005190268 |
| Devices in EUDAMED | 6 |
| Country of registration | Austria |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | OTTO BOCK HEALTHCARE PRODUCTS GMBH |
North American profile: Both markets. Otto Bock Healthcare Products GmbH is registered in both the United States and Canada.