Sanowa PlastoTec GmbH
DE-MF-000040380 · Germany · Leimen
Sanowa PlastoTec GmbH is registered in the European database on medical devices as a manufacturer, with 309 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
Devices declared under this manufacturer
- Bio Net 2 Embedding cassette - brown (loose)
- Bio Net 2 Embedding cassette - pink (loose)
- Bio Net Embedding cassette - dark green (loose) - coloured lid
- Bio Net Embedding cassette - neon green (loose)
- Bio Net Embedding cassette - turquoise (loose)
- Biopsie embedding cassette LMB aqua - stacked
- Biopsie embedding cassette LMB blue - stacked
- Biopsie embedding cassette LMB red - stacked
- Standard embedding cassette - orange (loose)
- Standard embedding cassette - turquoise (loose)
- Standard embedding cassette LMB green - stacked
- Uni-Link embedding cassette - white (loose)
Showing 12 of 309 declared devices.
Catalogue references include 110-005, 110-008, 111-002, 131-012, 131-017, 150-001.
European nomenclature codes declared: W05030501.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 309 |
| Country of registration | Germany |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 309 |
|---|---|
| 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. Sanowa PlastoTec GmbH was not found in either the U.S. or the Canadian register.