3TO GmbH
DE-MF-000017808 · Germany · Deisenhofen
3TO GmbH is registered in the European database on medical devices as a manufacturer, with 55 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 55 |
|---|
Devices declared under this manufacturer
- 3TO-Schlaufe
- 3TO-Spange mit 3TO-loop
- 3TO-loop
- COMBIped
- PODOSTRIPE
- PREMIOFORM Aktivelement 13 mm
- PREMIOFORM Aktivelement 16 mm
- PREMIOFORM FLUIDGEL
- podofix Komplettset
- podofix L
- podofix M
- podofix S
Showing 12 of 55 declared devices.
Catalogue references include 3131, 4110, 4140, 5120, 5320, 7110.
European nomenclature codes declared: Y061299.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 55 |
| 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 | 55 |
|---|---|
| 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. 3TO GmbH was not found in either the U.S. or the Canadian register.