STERIS IMS Limited
UK-MF-000042027 · United Kingdom · Northampton
STERIS IMS Limited is registered in the European database on medical devices as a manufacturer, with 1 500 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 1 500 |
|---|
Most frequent device types declared: Clamping Reusable Surgical Instruments, Cutting Reusable Surgical Instruments, Gouging Reusable Surgical Instruments, Grasping Reusable Surgical Instruments, Hammering Reusable Surgical Instruments.
Among these devices, 1 500 are declared reusable.
Authorised representative in the Union: STERIS Ireland Ltd.
Devices declared under this manufacturer
- NA
Showing 12 of 1 500 declared devices.
Catalogue references include PH191663, PH342850, PH584254, PH654796, PH70483, PH70641.
European nomenclature codes declared: L031310, L031306, L091302, L010499, L0205, L090401.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 1 500 |
| 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 | 1 500 |
|---|---|
| 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. STERIS IMS Limited was not found in either the U.S. or the Canadian register.