Tempur Sealy DACH GmbH
DE-MF-000048469 · Germany · Steinhagen
Tempur Sealy DACH GmbH is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 26 |
|---|
Most frequent device types declared: FOAM, Spring Mattresses.
Devices declared under this manufacturer
- Sealy Evolution 80x200x25
- Sealy Evolution Firm 90x190x25
- Sealy Evolution Firm 90x200x25
- Sealy Evolution Firm-140x200x25
- Sealy Generation 160x190x21
- Sealy Generation 160x200x21
- Sealy Generation 165x190x21
- Sealy Generation 200x200x21
- Sealy Generation 80x195x21
- Sealy Generation 90x200x21
- Sealy Illinois 80x200x25
- Sealy Vermont 80x190x25
Showing 12 of 26 declared devices.
Catalogue references include 70006765, 70006884, 70006924, 70006925, 70006933, 70007039.
European nomenclature codes declared: V0899.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. Tempur Sealy DACH GmbH was not found in either the U.S. or the Canadian register.