B.u.W. Schmidt GmbH
DE-MF-000022478 · Germany · Garbsen
B.u.W. Schmidt GmbH is registered in the European database on medical devices as a manufacturer, with 142 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 142 |
|---|
Most frequent device types declared: Bezug Vakuummatratze, Reparaturset PU blau, Rettungsmulde, Rettungstuch, Rollboard komplett faltbar.
Devices declared under this manufacturer
- Eis - Kompresse Schulter
- KIDDY-Bezug für Vakuummatratze
- Kinder - Armschiene Gr.2
- Reparatur-Set, farblich sortierte PVC-Folien-Abschnitte und Spezialkle
- Vacuform 2.0 100 x 125 cm Oberkörperlagerung
- Vacuform 2.0 30 x 70 cm Armlagerung
- Vacuform 2.0 40 x 40 x 50 cm Kopf - Dreieckskissen
- Vacuform 2.0 75 x 200 cm Schulter-OP ohne Kopfteil, inkl.Zusatzkissen
- Vacuform 2.0 75 x 200 cm Unterschenkel- und Fußchirurgie
- Vacuform 2.0 95/70 x 105 cm Oberkörper-Seitenlagerung nach MURPF
- Vacuform 2.0 QuickForm 80 x 100 cm
- Vacuform 2.0 Siliplus 75 x 100 cm
Showing 12 of 142 declared devices.
Catalogue references include 1190, 34365005, 3462005, 3466505, 37065005, 37065316.
European nomenclature codes declared: V080702, V0899, V080399, V08050101, V080504, V9099.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 142 |
| 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 | 142 |
|---|---|
| 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. B.u.W. Schmidt GmbH was not found in either the U.S. or the Canadian register.