Vernacare
GB-MF-000008063 · United Kingdom · Chorley
Vernacare is registered in the European database on medical devices as a manufacturer, with 132 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 132 |
|---|
Most frequent device types declared: 24000, 24001, 24002, 24003, 70650.
Among these devices, 4 are declared sterile.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- ALBERT™ Endo Tissue Retrieval Bag
- ALVITA COMFIFAST YELLOW 10.75CM X 1M XLARGE LIMBS
- AZOWRAP CREPE 900X900 GREEN
- AZOWRAP NON-WOVEN I/L 1370X1370 GRN/BLUE
- BERT Endo Tissue Retrieval Bag
- COMFIFAST BEIGE 17.5CM X 10M ADULT TRUNKS
- COMFIFAST MS GREEN 5CM X 10M SMALL/MED LIMBS
- COMFIFAST MS GREEN 5CM X 3M SMALL/MED LIMBS
- COMFIFAST MS RED 3.5CM X 10M SMALL LIMBS
- COMFIFAST YELLOW 10.75CM X 5M XLARGE LIMBS
- COMFIGAUZ SIZE 00 1.2CM X 20 METRE
- COMFIGAUZ SIZE 12 2.7CM X 20 METRE
Showing 12 of 132 declared devices.
Catalogue references include 24000, 92235N, CC14, F44, F55, T126.
European nomenclature codes declared: M0303010103, T0299, M0303010101, M03030103, S010301, S010302.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | Vernacare Ltd. (GB) · FDA 3002974712 |
| Devices in EUDAMED | 132 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 132 |
|---|---|
| Found in the U.S. device database | 4 |
| Share | 3.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | VERNACARE |
North American profile: Both markets. Vernacare is registered in both the United States and Canada.