Runfold Plastics Ltd
GB-MF-000010291 · United Kingdom · Liphook
Runfold Plastics Ltd is registered in the European database on medical devices as a manufacturer, with 26 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 26 |
|---|
Authorised representative in the Union: International Associates Auditing & Certification Limited.
Catalogue references include MMA-900-0005, MMA-900-0006, MMA-900-0080, MMA-900-0101, MMA-900-0102, MMA-900-0134.
European nomenclature codes declared: G02060303.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 26 |
| 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 | 26 |
|---|---|
| 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. Runfold Plastics Ltd was not found in either the U.S. or the Canadian register.