Medivance Instruments Limited
GB-MF-000024293 · United Kingdom · London
Medivance Instruments Limited is registered in the European database on medical devices as a manufacturer, with 24 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 24 |
|---|
Most frequent device types declared: Single, Twin, Twin (Black Edition).
Authorised representative in the Union: MedNet EC-REP GmbH.
Devices declared under this manufacturer
- Aluminium Oxide 29 µm Powder (Blue label)
- Aluminium Oxide 53 µm Powder (Red label)
- AquaCare
- AquaCare Foot Pedal (White)
- Ergo Foot Pedal Assembly (Black Edition)
- Feedlines and Tips (Plus Tips)
- Feedlines and Tips (Standard)
- Feedlines and Tips (iTips)
- Handpiece Black 0.6mm (Silver ring)
- Handpiece Black 0.8mm (Gold ring)
- Quick Release Twin Tube
- Quick Release Twin Tube (Black Edition)
Showing 12 of 24 declared devices.
Catalogue references include I/ASS 8008F, I/ASS 8009F, I/ASS 8020F, I/ASS 8021F, I/ASS 8188F, I/ASS 8189F.
European nomenclature codes declared: Q010199, Q01010403.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | MEDIVANCE INSTRUMENTS LTD. (GB) · FDA 3003982003 |
| Devices in EUDAMED | 24 |
| Country of registration | United Kingdom |
Device-level evidence
| Devices with a numeric GTIN | 24 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | MEDIVANCE INSTRUMENTS LTD. |
North American profile: Both markets. Medivance Instruments Limited is registered in both the United States and Canada.