NOBAMED Paul Danz AG
DE-MF-000000023 · Germany · Wetter (Ruhr)
NOBAMED Paul Danz AG is registered in the European database on medical devices as a manufacturer, with 1 277 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 277 |
|---|
Among these devices, 276 are declared sterile, 8 reusable.
Devices declared under this manufacturer
- MULLKOMPRESSEN 20x25 16FACH
- NOBA-TRANSFERTUCH 75x190 CM
- NOBACAST®-BLAU 7,5 CM 3,6M
- NOBADRAPE® KLEBETUCH 180x180CM 3-TEILIGE STREIFEN
- NOBAGLOVE® NITRIL classic M WEIß
- NOBAKAWA® 21 x 38 CM
- NOBARIGID® GESCHLOSSEN SIZE M
- NOBASHUCO® RUTSCHFEST
- NOBA® PFLEGETÜCHER
- RINGTUPFER Ø 3,5 CM
- RUDAFILM®-Steril 12x10CM
- RUDAKITAPE® NATUR 5 M 5,00 CM
Showing 12 of 1 277 declared devices.
Catalogue references include 071005, 073588, 430515, 620150, 675101, 801180.
European nomenclature codes declared: M0303010101, M0201020101, M03050202, M0201020102, M03030103, M0201020202.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 277 |
| 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 | 1 277 |
|---|---|
| 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. NOBAMED Paul Danz AG was not found in either the U.S. or the Canadian register.