Nippon Sanso Deutschland GmbH
DE-MF-000005116 · Germany · Düsseldorf
Nippon Sanso Deutschland GmbH is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 9 |
|---|
Devices declared under this manufacturer
- Kohlendioxid med.
Catalogue references include 001830, 004830, 006830, 008830, 010830, 030830.
European nomenclature codes declared: V0901.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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. Nippon Sanso Deutschland GmbH was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
G20 073553 0008 Rev. 01 | issued | 2028-07-03 |
G20 073553 0008 | amended | 2028-07-03 |