IM Med Ltd
GB-MF-000009796 · United Kingdom · Cambridge
IM Med Ltd is registered in the European database on medical devices as a manufacturer, with 9 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIb | 7 |
|---|---|
| Class IIa | 2 |
Most frequent device types declared: iM EZCept Detergent, iM Peracept.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- ProCare Med 10 E
- ProCare Med 10 E PAC
- iM EZCept
- iM Peracept 15 Disinfectant
- iM Peracept Duo A
- iM Peracept Duo B
- iM Peracept FC Disinfectant
- iM SafeCide Part One
- iM SafeCide Part Two
Catalogue references include 110050, 110500, 110502, 110505, 110525, 110525 / 9993028.
European nomenclature codes declared: D050101, D0801.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 9 |
| 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 | 9 |
|---|---|
| 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. IM Med Ltd was not found in either the U.S. or the Canadian register.