Sakura Finetek Europe B.V.
NL-MF-000023138 · Netherlands · Alpen aan den Rijn
Sakura Finetek Europe B.V. is registered in the European database on medical devices as a manufacturer, with 47 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| other | 47 |
|---|
Most frequent device types declared: Tissue-Tek® Uni-Cassette® Standard Cassettes, Tissue-Tek® Paraffin Wax TEK III, Tissue-Tek® Glas™ Coverslips, Tissue-Tek® Glas™, Tissue-Tek® Tissue-Clear® Xylene Substitute.
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | SAKURA FINETEK EUROPE B.V. (NL) · FDA 9614585 |
| Devices in EUDAMED | 47 |
| Country of registration | Netherlands |