Bingold GmbH + Co. KG
DE-MF-000016561 · Germany · Hamburg
Bingold GmbH + Co. KG is registered in the European database on medical devices as a manufacturer, with 288 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 288 |
|---|
Devices declared under this manufacturer
- Bingold Latex BLACK
- Bingold Nitril 35
- Bingold Nitril 35Med
- Bingold Nitril 50.300
- Bingold Nitril 50PLUS
- Clean and Clever
- Kolibri
- Kolibri Premium Latex
- Medisoft Care
- Medisoft care
- Tapira
- aximed pro Latex
Showing 12 of 288 declared devices.
Catalogue references include 10000524, 1130060, 2134071, 2232404, 602201, 634604.
European nomenclature codes declared: T01020204, T010201, T01020201, T0205, T0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 288 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 288 |
|---|---|
| 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: Neither register. Bingold GmbH + Co. KG was not found in either the U.S. or the Canadian register.