nal von minden GmbH
DE-MF-000013321 · Germany · Moers
nal von minden GmbH is registered in the European database on medical devices as a manufacturer, with 215 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- MultiDip 7-3X Test
- NADAL® Gonorrhea Test
- NADAL® Strep A Plus Test
- NADAL® Strep A Test
- NADAL® Strep B
- nal von minden Drug-Screen® AMP 1000 Test
- nal von minden Drug-Screen® BUP 10 Test
- nal von minden Drug-Screen® COC 300 Test
- nal von minden Drug-Screen® Multi 11TE Test
- nal von minden Drug-Screen® Multi 11TN Test Barcoded
- nal von minden Drug-Screen® Multi 7TA Test
- nal von minden Drug-Screen® THC 50 Test
Showing 12 of 215 declared devices.
Catalogue references include 101004, 102005, 103071S-25, 104114, 104214BA, 232001.
European nomenclature codes declared: W0102160511, W0102160599, W0105090103, W0102160508, W0102160505, W0102160502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 215 |
| 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 | 9 |
|---|---|
| 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. nal von minden GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
IX 1034230-2 | issued | 2031-03-02 |
HX 1034230-1 | issued | 2029-02-06 |