Albert Browne Limited
GB-MF-000017372 · United Kingdom · Leicester
Albert Browne Limited is registered in the European database on medical devices as a manufacturer, with 125 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 125 |
|---|
Most frequent device types declared: Bowie Dick Test Pack, Endoscope test devices-HexaLumen, Helix Load Test, Mediwrap, Steam Tape.
Authorised representative in the Union: STERIS Ireland Ltd.
Devices declared under this manufacturer
- Browne
- Celerity
- Eschmann
- Flexislide
- Isapor
- Mediwrap Blanket
- Mediwrap Legging
- Mediwrap Sleeping Bag
- Revital-Ox Resert
- TST Control
- Top Dent and Browne
- VERIFY
Showing 12 of 125 declared devices.
Catalogue references include 105025, 121184, 2317, 2341, 3804, 3805.
European nomenclature codes declared: Z12011385, T0399, Y1299.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ALBERT BROWNE LTD. (GB) · FDA 8021896 |
| Devices in EUDAMED | 125 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 125 |
|---|---|
| Found in the U.S. device database | 8 |
| Share | 6.4 % |
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. Albert Browne Limited is registered in the United States but was not found in the Canadian register.