Serrix B.V
NL-MF-000005882 · Netherlands · Amsterdam
Serrix B.V is registered in the European database on medical devices as a manufacturer, with 36 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 36 |
|---|
Devices declared under this manufacturer
- Mycoben Pie de atleta - 15 mL Brushtube
- Mycosan Fungal Nail treatment kit - 5mL Brushtube
- Mycosan Grzybica Paznokci Zestaw do leczenia - 5mL Brushtube
- Mycosan Kalknagel Behandelset - 10mL Brushtube
- Mycosan Körömgomba Kezelési készlet - 10mL Brushtube
- Mycosan küüneseene ravikomplekt - 5mL Brushtube
- Mycosan Αντιμετώπιση των Μυκήτων των Νυχιών - 5mL Brustube + 8mL Na
- Mycosana Pés Pé de Atleta - 15 mL Brushtube
- Mycosana Unhas Fungos das Unhas Kit de tratamento - 5mL Brushtube
- Pirolam Derm Leczenie grzybicy paznokcia - 4mL Pen
- SoreFix Ehkäisevä Huuliherpesvoide - 8 mL Jar
- SoreFix Rescue Koortslipcrème - 6 mL Tube
Showing 12 of 36 declared devices.
Catalogue references include L030FI, L040BE, M030IE, M030PL, M030PT, M040NL.
European nomenclature codes declared: V9099, M0410.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 36 |
| Country of registration | Netherlands |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 36 |
|---|---|
| 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. Serrix B.V was not found in either the U.S. or the Canadian register.
Notified body certificates
| Certificate | Status | Expiry |
|---|---|---|
BE23/00000172 | supplemented | 2028-06-19 |