Pronova Laboratories BV
NL-MF-000001486 · Netherlands · Muiden
Pronova Laboratories BV is registered in the European database on medical devices as a manufacturer, with 13 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 13 |
|---|
Most frequent device types declared: CT10XX100, FW10XX100, LN10XX100, NC10XX100, PN10XX100.
Among these devices, 9 are declared active.
Devices declared under this manufacturer
- Coldner Keelspray
- Dr. Scholl's Freeze Away MAX EXPERTTREATMENT Traitement Verrues Cryoth
- Dr. Scholl's Freeze Away MAX Fodvorte- Og Vortefjerner
- Dr. Scholl's Freeze Away MAX Traitement Verrues Cryothérapie
- Dr. Scholl's Freeze Away MAX Trattamento Rimozione Verruche
- Dr. Scholl's Freeze Away MAX Verruca & Wart Remover
- Dr. Scholl's Freeze Away MAX Zestaw Do Usuwania Kurzajek I Brodawek
- Forwarts Wrattenverwijderaar
- Forwarts Wrattenverwijderaar / Élimine les Verrues / Warzenentferner
- Nailclin Schimmelnagelbehandeling
- Prevner Koortslipcrème
- WEPA Warzenvereiser
Showing 12 of 13 declared devices.
Catalogue references include CT10NLXXX, FW10BE100, FW10DE100, FW10FRM100, FW10FRP100, FW10NORD100.
European nomenclature codes declared: V0999, M9002, V901001, M0410.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | PRONOVA LABORATORIES BV (NL) · FDA 3015733082 |
| Devices in EUDAMED | 13 |
| Country of registration | Netherlands |
Device-level evidence
| Devices with a numeric GTIN | 13 |
|---|---|
| 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. Pronova Laboratories BV is registered in the United States but was not found in the Canadian register.