Reintex GmbH
DE-MF-000041775 · Germany · Ketsch
Reintex GmbH is registered in the European database on medical devices as a manufacturer, with 63 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 63 |
|---|
Devices declared under this manufacturer
- 2042W Einmal-Kissen-Bezüge
- 2062WL Einmal-Kissen-Bezüge
- RTKS-SET 700g
- RTPTL 48/110 Einmal-Papierlaken - 48-fach verstärkt
- RTPTL 50 Einmal-Papierlaken - 50-fach verstärkt
- RTUBT Einweg-Patienten- Umbettungstuch / Umbettungslaken
- RTW 190 Einwegdecke
- RTWK40 Einmalkissen
- RTWK80 Einmalkissen
- RUB 300 Einwegdecke
- RUB 500XL Einwegdecke
- VLBL 120 Einmal-Vlieslaken
Showing 12 of 63 declared devices.
Catalogue references include RTKS-SET 700g, RTUBT, RTW 190, RTWK40, RUB 300, RUB 500XL.
European nomenclature codes declared: V08068099, V080399, V080505.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 63 |
| 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 | 63 |
|---|---|
| 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. Reintex GmbH was not found in either the U.S. or the Canadian register.