Anaesthetic Medical Systems Ltd
GB-MF-000016544 · United Kingdom · Cheshire
Anaesthetic Medical Systems Ltd is registered in the European database on medical devices as a manufacturer, with 20 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 20 |
|---|
Most frequent device types declared: Infusion set.
Among these devices, 20 are declared sterile.
Authorised representative in the Union: MD REPS Ltd.
Devices declared under this manufacturer
- A12PD-Set
- A2-Set
- A2-Set NFV
- A2-Set No Clamp
- A22BL-Set
- A23BL-Set
- A23LV-Set
- A2L-Set
- A3-Set
- A3-Set No Clamp
- A33BL-Set
- A4-Set
Showing 12 of 20 declared devices.
Catalogue references include 7200A, 7200ANF, 7200L, 7300A, 7430BL, 8200A.
European nomenclature codes declared: A070103.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 20 |
| Country of registration | United Kingdom |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 20 |
|---|---|
| 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: Neither register. Anaesthetic Medical Systems Ltd was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
28620126993 | issued | 2027-05-19 |