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
Most frequent device types declared: Tissue-Tek® AutoWrite® Non-Adhesive Ground Edges 90° Clipped Corner Sl, Tissue-Tek® Glas™, Tissue-Tek® Glas™ Coverslips, Tissue-Tek® Paraffin Wax TEK III, Tissue-Tek® Tissue-Clear® Xylene Substitute.
Devices declared under this manufacturer
- Tissue-Tek® AutoWrite® Adhesive Ground Edges 90° Clipped Corner Slides
- Tissue-Tek® AutoWrite® Non-Adhesive Ground Edges 90° Clipped Corner Sl
- Tissue-Tek® Glas™
- Tissue-Tek® Glas™ Coverslips, 24 x 60 mm
- Tissue-Tek® Glas™ Mounting Medium
- Tissue-Tek® Glas™ Pertex
- Tissue-Tek® Paraffin Wax TEK III
- Tissue-Tek® Paraffin Wax TEK IV
- Tissue-Tek® Uni-Cassette® Standard Cassettes, Blue
- Tissue-Tek® Uni-Cassette® Standard Cassettes, Green
- Tissue-Tek® Uni-Cassette® Standard Cassettes, Pink
- Tissue-Tek® Uni-Cassette® Standard Cassettes, White
Showing 12 of 47 declared devices.
Catalogue references include 4170, 4523, 8155, 8156, 9580, 9582.
European nomenclature codes declared: W05030501, W0503900201, W01030704, W01030799, W0503900202, W01030706.
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 |
Device-level evidence
| Devices with a numeric GTIN | 47 |
|---|---|
| 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: United States only. Sakura Finetek Europe B.V. is registered in the United States but was not found in the Canadian register.