J RIPOLL SL
ES-MF-000001256 · Spain · Algete
J RIPOLL SL is registered in the European database on medical devices as a manufacturer, with 179 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 179 |
|---|
Most frequent device types declared: ABG, ACO, ACOV, ARS60, EUGK.
Devices declared under this manufacturer
- 040 Clear 25 Ud Dentaflux
- Cubeta flúor dobles grandes Royal
- Cubetas de impresión sólidas KIT 10, no perforadas
- Cubetas de impresión sólidas Nº4 superior, no perforadas
- Double large fluoride tray Dentaflux
- Etching gel - Phosphoric acid 37% 1 syringe of 60g 5 empty syringes (3
- HEMOCOR
- Hilo de retracción tejido Nº1 Dentaflux
- Hilo retracción Nº2 Royal
- Sobre 10 copas goma Dentaflux
- THERMOPLASTIC SHEETS 040 Clear 25 Ud Bestdent
- cepillos profilaxis bolsa 100 uds Royaldent
Showing 12 of 179 declared devices.
Catalogue references include 040CL, 040CLB, 060CLDO, 060MDO, 10CO, FDG.
European nomenclature codes declared: Q010499, Q01010402, Q010503, Q010204, Q0101010299, Q0199.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 179 |
| Country of registration | Spain |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 179 |
|---|---|
| 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. J RIPOLL SL was not found in either the U.S. or the Canadian register.