Albert Kerbl GmbH
DE-MF-000007708 · Germany · Buchbach
Albert Kerbl GmbH is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 27 |
|---|
Most frequent device types declared: 153070-153074, 15355-15358, Latex Top S.
Devices declared under this manufacturer
- Latex Classic L
- Latex Classic M
- Latex Top L
- Latex Top S
- Nitril Classic L
- Nitril Classic M
- Nitril Classic XL
- Nitril Classic XXL
- Nitril Profi S
- Nitril Sensitive
- Nitril Sensitive L
- Nitril Sensitive M
Showing 12 of 27 declared devices.
Catalogue references include 153067, 153069, 153073, 153074, 15340, 15357.
European nomenclature codes declared: T01020204, T010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 27 |
| 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 | 27 |
|---|---|
| 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. Albert Kerbl GmbH was not found in either the U.S. or the Canadian register.