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: Polyethylene fenestrated tracheostomy cannulas. Size 6., Silicone fenestrated tracheostomy cannulas. 1 Piece. Size 5., Silicone laryngectomy cannulas with head adapted for HME filters. 1 Pi, Silicone laryngectomy cannulas with head adapted for HME filters. Size, Silicone laryngectomy cannulas. Standard. 1 Piece. Size 4..
Devices declared under this manufacturer
- F.CHINER
Showing 12 of 49 declared devices.
Catalogue references include L1020855FA, T1030965C15, T2061277NEF, T3041055, T3041063HME, T30511105F.
European nomenclature codes declared: R0105010101.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 49 |
| 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 | 49 |
|---|---|
| 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. Francisco Chiner SL was not found in either the U.S. or the Canadian register.