Rosa Toifl & Co GmbH
AT-MF-000020516 · Austria · Wien
Rosa Toifl & Co GmbH is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Among these devices, 3 are declared sterile.
Catalogue references include 23100, 23101, 23103, 23104, 23160, 43350.
European nomenclature codes declared: T02010101, T030102, T020401, T0202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| Country of registration | Austria |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 9 |
|---|---|
| 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. Rosa Toifl & Co GmbH was not found in either the U.S. or the Canadian register.