Meditech Endoscopy Limited
GB-MF-000014143 · United Kingdom · Basildon, Essex
Meditech Endoscopy Limited is registered in the European database on medical devices as a manufacturer, with 6 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 6 |
|---|
Most frequent device types declared: INOV8-051.
Authorised representative in the Union: Elara Pharmaservices Europe Ltd.
Devices declared under this manufacturer
- ColoGrip
- PrioriTag
- StageOne (Enzymatic)
- StageOne (Neutral)
- Tote Timer
- ValveSafe
Catalogue references include INOV8-001, INOV8-009, INOV8-009E, INOV8-014, INOV8-048, INOV8-051.
European nomenclature codes declared: V9099, Z12011301, S010499.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MEDITECH ENDOSCOPY LTD (GB) · FDA 3011346938 |
| Devices in EUDAMED | 6 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 6 |
|---|---|
| Found in the U.S. device database | 1 |
| Share | 16.7 % |
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: United States only. Meditech Endoscopy Limited is registered in the United States but was not found in the Canadian register.