Yeti Dentalprodukte GmbH
DE-MF-000005557 · Germany · Engen
Yeti Dentalprodukte GmbH is registered in the European database on medical devices as a manufacturer, with 27 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 27 |
|---|
Devices declared under this manufacturer
- Bißnehmewachs Gelb (weich) Zitrone
- Bißnehmewachs Grün (mittel) Apfel
- Bißnehmewachs Rosa (hart) Erdbeer
- Bißregistrierungswachs rosa hart 2,0 mm
- Bißwälle Grün (mittelhart) Apfel 96 St.
- Bißwälle Orange (mittelhart) 96 St.
- Bißwälle Rosa (hart) Erdbeer, 96 St.
- Bißwälle rosa (sehr hart) 100 St.
- K2 Opaquer Pulver O-A2, 15g.
- Metallfolienwachs braun, 4mm, 60St.
- SPEZIAL Modellierw. Sommer Rosa 1,5mm
- SPEZIAL Modellierw. Winter Rosa 1,25mm
Showing 12 of 27 declared devices.
Catalogue references include 605-0060, 611-0100, 613-0100, 613-0490, 653-0500, 653-2500.
European nomenclature codes declared: Q01020199, P01020101.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | YETI DENTALPRODUKTE GMBH (DE) · FDA 3006235664 |
| Devices in EUDAMED | 27 |
| Country of registration | Germany |
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: United States only. Yeti Dentalprodukte GmbH is registered in the United States but was not found in the Canadian register.