Adelphi (Tubes) Limited
UK-MF-000042179 · United Kingdom · Haywards Heath
Adelphi (Tubes) Limited is registered in the European database on medical devices as a manufacturer, with 8 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 8 |
|---|
Most frequent device types declared: Sterile Nitrogen filled vial.
Among these devices, 8 are declared sterile.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Anoxos 10ml Sterile Nitrogen filled vial
- Anoxos Sterile Nitrogen filled vial
- Anoxos Sterile Nitrogen filled vials
Catalogue references include VNS02X2, VNS10RB, VNS10RTTB32, VNS10TTB3T1+I2, VNS10TTB3T1+R, VNS20RTTB3RB.
European nomenclature codes declared: V0499.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 8 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 8 |
|---|---|
| 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. Adelphi (Tubes) Limited was not found in either the U.S. or the Canadian register.