JRI Orthopaedics Ltd
GB-MF-000007529 · United Kingdom · Sheffield
JRI Orthopaedics Ltd is registered in the European database on medical devices as a manufacturer, with 702 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 444 |
|---|---|
| Class I | 238 |
| Class IIb | 20 |
Among these devices, 258 are declared sterile, 258 implantable, 383 reusable.
Authorised representative in the Union: CMC Medical Devices & Drugs SL.
Devices declared under this manufacturer
- ACE® Dual Mobility Instrument Tray
- ACE® Primary Instrument Tray
- Bipolar Head Assembly Jig
- Cement Chisel - 9mm 15ø
- Ceramic Liner Removal Tool Handle
- Cup Removal Tool CSF Plus Poly Insert - Size 48mm
- Femoral Canal Finder Rasp - Left Hand
- Humeral Resection Plate
- Intramedullary Reamer - 15mm
- Osteotome - 20mm Wide Blade
- Pelvic Lever - 26mm x 330mm
- Screw Depth Gauge
Showing 12 of 702 declared devices.
Catalogue references include 10-09-42, 14-99-64, 15-15-61, 170-46-07, 286-33-48, 433-02-10.
European nomenclature codes declared: P090804010201, L098099, L091101, L091102, L091104, P090803040101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 702 |
| 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 | 702 |
|---|---|
| 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. JRI Orthopaedics Ltd was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
MDR 741731 | supplemented | 2027-03-29 |