Globus (Shetland) Ltd
GB-MF-000007384 · United Kingdom · manchester
Globus (Shetland) Ltd is registered in the European database on medical devices as a manufacturer, with 158 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 158 |
|---|
Most frequent device types declared: EMG460, NX520, TX324, TX424, TX4525.
Authorised representative in the Union: Globus EMEA Ltd.
Devices declared under this manufacturer
- Benchmark
- Consumable Solutions
- HAIKA
- Haika
- Keepsafe
- SKYTEC
- SKYTEC Elements
Showing 12 of 158 declared devices.
Catalogue references include HAK52, SKG00324IF, SKG00424DJ, SKG00524BH, SKG00530EH, SKG00630BD.
European nomenclature codes declared: T01020204, T01020201, T020604.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 158 |
| 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 | 158 |
|---|---|
| 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. Globus (Shetland) Ltd was not found in either the U.S. or the Canadian register.