ANTITOXIN GmbH
DE-MF-000008156 · Germany · Bammental
ANTITOXIN GmbH is registered in the European database on medical devices as a manufacturer, with 56 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- AHG serum blend
- Anti-AB monoclonal, IgM clones: ES-15, ES-4
- Anti-C monoclonal, human IgM clone: MS-273
- Anti-D blend monoclonal, human IgG+IgM clones: MS-26, TH-28
- Anti-Fya Coombs-reactive, polyclonal, human
- Anti-Jkb Coombs-reactive, polyclonal, human
- Anti-Jkb for card method, monoclonal, human IgM clone: MS-8
- Anti-Jkb monoclonal, human IgM clone: MS-8
- Anti-M for card method monoclonal, mouse Clone: LM110/140
- Anti-M for card method monoclonal, mouse clone: LM110/140
- Anti-Wr(a) monoclonal IgG
- Anti-cellano, Coombs-reactive, polyclonal, human
Showing 12 of 56 declared devices.
Catalogue references include 01.021-05, 01.141-10, 01.179-05, 02.053-02, 213181, 421605.
European nomenclature codes declared: W01030399, W0103030501, W0103030202, W0103030102, W0103030201, W0103030304.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 56 |
| 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 | 53 |
|---|---|
| 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. ANTITOXIN GmbH was not found in either the U.S. or the Canadian register.