KOB GmbH
DE-MF-000005043 · Germany · Wolfstein
KOB GmbH is registered in the European database on medical devices as a manufacturer, with 489 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 489 |
|---|
Devices declared under this manufacturer
- Askina Elast Fine
- Askina Zinkleimbinde
- Bi-Grip
- Chemifix
- Elasti-Fix
- Eurofix
- GIPHAR BANDE DE CONTENTION
- LASTINEIR
- Langzugbinde
- Long-Stretch Compression Bandage Fine
- Primacrepe
- Urgozink elast
Showing 12 of 489 declared devices.
Catalogue references include 220003, 3105, 510504, 755025BL, 811345, 9052216.
European nomenclature codes declared: M0303010201, M030402010101, M0304010102, M030402020101, M0303010101, M03030199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | KOB GmbH (DE) · FDA 8010200 |
| Devices in EUDAMED | 489 |
| Country of registration | Germany |
Device-level evidence
| Devices with a numeric GTIN | 489 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Not found in the Canadian register |
|---|
⚠️ Canada lists no Class I devices at all — what that excludes.
North American profile: United States only. KOB GmbH is registered in the United States but was not found in the Canadian register.