Francisco Chiner SL
ES-MF-000019696 · Spain · Picanya
Francisco Chiner SL is registered in the European database on medical devices as a manufacturer, with 49 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 34 |
|---|---|
| Class IIb | 15 |
Most frequent device types declared: Silicone fenestrated tracheostomy cannulas. 1 Piece. Size 7., Silicone fenestrated tracheostomy cannulas. 1 Piece. Size 6., Silicone fenestrated tracheostomy cannulas. 1 Piece. Size 8., Polyethylene fenestrated tracheostomy cannulas. Size 6., Silicone fenestrated tracheostomy cannulas. 1 Piece. Size 5..
No authorised representative is recorded for these devices. For a manufacturer established outside the Union that would be unusual; for one established inside it, it is normal.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 49 |
| Country of registration | Spain |
⚠️ Absence here is not proof of absence from the market. A manufacturer may reach the United States through a distributor registered under its own name, or under a corporate name we could not match. We publish what we measured, not what we inferred.