DNTL Nordic ApS
DK-MF-000013594 · Denmark · Nykøbing Sj.
DNTL Nordic ApS is registered in the European database on medical devices as a manufacturer, with 41 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 41 |
|---|
Devices declared under this manufacturer
- EDTA-C 17 %, 500 ml
- EDTA-C 17%, 500 ml
- Klorhexidin 0,2% med mint, 250 ml
- Klorhexidin 0,2% mundskyllevæske, 250 ml
- Natriumhypochlorit 5 %, 1000 ml
- Nordenta Klorhexidin 0,2% MINT mundskyllevæske, 250 ml
- Nordenta Klorhexidin 0,2% mundskyllevæske, 250 ml
- Nordenta Natriumhypochlorit 2,5 %, 1000 ml
- Orbis Hypodest 3 %, Sodium hypochlorite 3 %, 500 ml
- Orbis Hypodest 5 %, Natriumhypochlorit 5 %, 1000 ml
- Orbis Klorohex mundskyl Klorhexidin 0,2% med mynte, 250 ml
- Orbis OxyDes 3% brintoverilte 3% 1000 ml
Showing 12 of 41 declared devices.
Catalogue references include 105478, 111140, 113729, 3067, 55520, DN103.
European nomenclature codes declared: Q010199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 41 |
| Country of registration | Denmark |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 41 |
|---|---|
| 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. DNTL Nordic ApS was not found in either the U.S. or the Canadian register.