Sterilin Ltd
GB-MF-000026916 · United Kingdom · Newport
Sterilin Ltd is registered in the European database on medical devices as a manufacturer, with 7 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Among these devices, 7 are declared sterile.
Authorised representative in the Union: NUNC A/S.
Devices declared under this manufacturer
- 100ML CONT PTD LAB D/BAG I/W
- 250ML CONT PTD LABEL D/BAG I/W
- 250ML CONTAINER NO LABEL IRRAD
- 250ML CONTAINER PLAIN LABEL IR
- 30ML PTD LAB D/BAG I/W IRR
- 30ML UNI CONT RED CAP T/PK IRR
- 30ML UNI NO LBL RED QS CAP IRR
Catalogue references include 128AR/IRR, 128BR/1/IRR, 128DB/IRR, 185DB/IRR, 190A/IRR, 190C/IRR.
European nomenclature codes declared: W050301020102.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 7 |
| 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 | 7 |
|---|---|
| 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. Sterilin Ltd was not found in either the U.S. or the Canadian register.