Transatlantic HG Stolpe & Co. mbH
DE-MF-000009432 · Germany · Neu-Anspach
Transatlantic HG Stolpe & Co. mbH is registered in the European database on medical devices as a manufacturer, with 75 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 75 |
|---|
Most frequent device types declared: D100100, Patiententransporthilfe.
Devices declared under this manufacturer
- Ersatz-Endleisten-Set Professional Slim
- Ersatz-Rolltuch-Set Professional Slim
- Ersatz-Rolltuch-Set Silver Special
- Transafix Fixierstreifen No.2
- Transafix Nasalband mit Klett
- Transafix No.1 Monatspackung (6 St. Fixierstreifen)
- Transafix No.3 Monatspackung (5 St. Fixierstreifen)
- Transaroll Blueboard Standard
- Transaroll Eco-Board
- Transaroll Professionalboard Standard
- Transaroll Silverboard Mini
- Transaroll Silverboard Special
Showing 12 of 75 declared devices.
Catalogue references include 4400421SET, 4401100, 4500029, 4500034, 8210300, 8500350.
European nomenclature codes declared: V080504, H900299, V08050199, V0899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 75 |
| 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 | 75 |
|---|---|
| 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. Transatlantic HG Stolpe & Co. mbH was not found in either the U.S. or the Canadian register.