Medicina Limited
UK-MF-000041402 · United Kingdom · Bolton
Medicina Limited is registered in the European database on medical devices as a manufacturer, with 116 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 94 |
|---|---|
| Class IIb | 22 |
Most frequent device types declared: AP10/30, CG4/40, CG5/50, CG6/100, LHE01LD.
Among these devices, 104 are declared sterile, 45 with a measuring function.
Authorised representative in the Union: HMC PREMEDICAL S.P.A..
Devices declared under this manufacturer
- ACElok Dressing
- Ace Stopper
- Ace Stopper and Dressing
- Blunt Fill Needle
- ENFit Low Dose Enteral Syringe
- ENFit Low Dose reusable Enteral Syringe
- ENFit reusable Enteral Syringe
- Luer Lock IV Syringe
- Luer Slip IV Syringe
- Luer Slip IV Syringe (Eccentric)
- Nasogastric tubes for short term use
- Oral tip syringe
Showing 12 of 116 declared devices.
Catalogue references include AP10/30, CG4/40, CG5/50, CG6/100, LHE01LD, RT12/100C.
European nomenclature codes declared: G02020101, A020199, Y0999, A020299, V0599, A0199.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MEDICINA LTD (GB) · FDA 3008432385 |
| Devices in EUDAMED | 116 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 116 |
|---|---|
| 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: United States only. Medicina Limited is registered in the United States but was not found in the Canadian register.