Anetic Aid Ltd
GB-MF-000011932 · United Kingdom · Havant
Anetic Aid Ltd is registered in the European database on medical devices as a manufacturer, with 77 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 77 |
|---|
Authorised representative in the Union: EU-UK Authorised Representative Ltd.
Devices declared under this manufacturer
- Clamp - Universal (Socket & Rail) - Handwheel - for UK / EU / Swiss Si
- Doughnut Headring Adult
- Lateral Support c/w Pad
- QA3 Ophthalmic Stretcher with Pressure Care Mattress
- QA3 Patient Stretcher - with Pressure Care Mattress
- QA3 Powered Emergency Department Stretcher - with Pressure Care Mattre
- QA3 Pressure Care Mattress - for QA3 Ophthalmic
- QA3 Pressure Care Mattress - for QA3 v3.0 / v4.0 - Serial No. 11681 On
- QA4 Leg Section - Split Leg Positioner - with EU Side Bar
- QA4 Pressure Care Mattress - Upper & Lower Torso Section
- Reusable Tourniquet Cuff - Arm - IVRA / Bier's Block - 460mm / 18\
- Six-use Day Tourniquet Cuff - Large Arm / Small Leg - Narrow - 610mm /
Showing 12 of 77 declared devices.
Catalogue references include 10200, 21110, 21118, 21126, 21359, 25430.
European nomenclature codes declared: V9099, Z12011299, Y1299, V080701, Z12030399, M0399.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | ANETIC AID LTD (GB) · FDA 3006975482 |
| Devices in EUDAMED | 77 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 77 |
|---|---|
| Found in the U.S. device database | 11 |
| Share | 14.3 % |
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. Anetic Aid Ltd is registered in the United States but was not found in the Canadian register.