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: MT-AR-000000234.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 159 |
| Country of registration | United Kingdom |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.