3M Deutschland GmbH (Medical)
DE-MF-000011641 · Germany · Neuss
3M Deutschland GmbH (Medical) is registered in the European database on medical devices as a manufacturer, with 136 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 136 |
|---|
Most frequent device types declared: N1675W, N2005P, V12M3Z24, V1714AS, V17T27O1.
Among these devices, 8 are declared sterile, 3 active.
Devices declared under this manufacturer
- 3M™ Nexcare™ Bandages Waterproof universal
- 3M™ Nexcare™ ColdHot Therapy Pack, Teddy
- M|Plast Pflaster wasserabweisend
- Nexcare™ Athletic Wrap
- Nexcare™ Bandages Breathable Universal
- Nexcare™ Bandages Happy Kids
- Nexcare™ Blood Stop
- Viscoplast™ Gaza opatrunkowa jałowa
- Viscoplast™ Opti-plast Junior
- Viscoplast™ Poloflex Przylepiec Elastyczny
- Viscoplast™ Tamujący Krwawienie
- Viscoplast™ plastry dzecięce MIX
Showing 12 of 136 declared devices.
Catalogue references include 5203.502, N1130ASD01W, N1579, N1730AS, V1714AS, V3-20-2G.
European nomenclature codes declared: M04010101, M04010102, M9001, M050101, M020199, M040303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 136 |
| 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 | 136 |
|---|---|
| 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. 3M Deutschland GmbH (Medical) was not found in either the U.S. or the Canadian register.