Hugh Steeper Limited
GB-MF-000010196 · United Kingdom · Leeds
Hugh Steeper Limited is registered in the European database on medical devices as a manufacturer, with 1 432 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 1 432 |
|---|
Most frequent device types declared: ASC****.
Among these devices, 278 are declared active.
Authorised representative in the Union: Emergo Europe B.V..
Devices declared under this manufacturer
- 8 1/4in Myo Kinisi Myoelectric hand LEFT with N A wrist
- Adapter Plate Flat 50mm
- Cosmetic Hand Right Male Adult - Long Fingers Extended Reinforced Wi
- ELECTRODE SEAL IN KIT
- Espire Elbow Classic- Left- Caucasian- Medial Dial- Standard
- Espire Elbow Classic- Right- Caucasian- Medial Dial- Small
- Espire Elbow Hybrid- Left- Black Carbon Finish- Medial Dial- Standard
- Espire Elbow Hybrid- Right- Silver- Medial Dial- Small
- ON/OFF SWITCH AND CHARGE PORT
- S-Charge Display Kit
- SKINERGY PLUS CT 26/27LS E7
- SPLIT TF SKIN+ 24/25 LT S E1
Showing 12 of 1 432 declared devices.
Catalogue references include B11090REIN, B27804, EEC-RCMS, EEH-RSMS, ELSK, KIN825LNA.
European nomenclature codes declared: Y061899, Y062499, Y061803, Y062403, Y061809, Y061815.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | HUGH STEEPER LTD (GB) · FDA 9612243 |
| Devices in EUDAMED | 1 432 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 1 432 |
|---|---|
| Found in the U.S. device database | 9 |
| Share | 0.6 % |
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: United States only. Hugh Steeper Limited is registered in the United States but was not found in the Canadian register.