Perfection Plus
GB-MF-000023781 · United Kingdom · United Kingdom (excl. Northern Ireland)
Perfection Plus is registered in the European database on medical devices as a manufacturer, with 159 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 159 |
|---|
Most frequent device types declared: Self Seal Sterilisation Pouches.
Among these devices, 53 are declared active.
Authorised representative in the Union: Advena Limited.
Devices declared under this manufacturer
- Eco+
- Orbis
- PerfectEtch-E Blue 60g Syringe & 50 tips
- Perfection Plus
- Perfection Plus Cotton Rolls
- Perfection Plus Eco+ Probe
- Perfection Plus Mouthwash Tablets
- Prophy+ Brushes Bristle RA pk 720
- Prophy+ Latex Free Cups Screw In Blue Hard pk 720
- Prophy+ Latex Free Cups Screw In Pink Soft pk 50
- Prophy+ Latex Free Cups Screw In Pink Soft pk 720
- Prophy+ Latex Free Cups Snap On Purple Medium pk 720
Showing 12 of 159 declared devices.
Catalogue references include 005/5601, 005/6103, 005/6202, 010/0006, 010/0160, 085/0016.
European nomenclature codes declared: Q010502, S01010101, Q01010401, Q019003, Q01010403, Q019004.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 159 |
| 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 | 159 |
|---|---|
| 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. Perfection Plus was not found in either the U.S. or the Canadian register.