Franz Mensch GmbH
DE-MF-000021137 · Germany · Buchloe
Franz Mensch GmbH is registered in the European database on medical devices as a manufacturer, with 367 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 367 |
|---|
Most frequent device types declared: Disposable blankets Plus, Examination gloves | synthetic rubber, Underpads for beds, with adhesive tape.
Devices declared under this manufacturer
- Bouffant caps Bettina Light | PP
- Chemical protection gloves Super High Risk | nitrile
- Einmal-Handschuhe aus Nitril
- Examination gloves Safe Virus | nitrile
- Face masks type II, 3-ply | PP, ties
- Gown with knitted cuffs | SMS
- Gowns with closed neck tie | PP/PE, partly laminated
- Nitrile gloves Extra Safe Super Stretch | powder-free
- Nitrile gloves Safe Fit | powder-free
- Nitrile gloves Safe Light | powder-free
- Nitrile gloves Safe Long Light | powder-free
- Nitrile gloves Safe Premium | powder-free
Showing 12 of 367 declared devices.
Catalogue references include 12649S, 261708, 27008, 270092, 27029, 27060.
European nomenclature codes declared: T01020204, T0205, T01020201, T0207, T020604, T010201.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 367 |
| 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 | 367 |
|---|---|
| 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. Franz Mensch GmbH was not found in either the U.S. or the Canadian register.