INTERmedic Arfran s.a.
ES-MF-000038662 · Spain · Madrid
INTERmedic Arfran s.a. is registered in the European database on medical devices as a manufacturer, with 33 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIb | 30 |
|---|---|
| Class IIa | 3 |
Most frequent device types declared: 1064DUAL, 980DUAL, CDL, LAFIB, M1064.
Among these devices, 1 are declared sterile, 32 reusable, 23 active.
Devices declared under this manufacturer
- EndoDefine 1470
- Gynelase Plus
- Laser fiber SiSiPol-Silicone 320mic
- Lipodefine 1470
- Lipodefine 980
- MULTIDIODE One DeYAG 190 DUAL
- MULTIDIODE One HP240 DUAL
- Multidiode Endo Laser 1470
- Multidiode Surgical Series 4G
- Silklase
- Silklase Infinity
- Silklase Infinity Plus
Showing 12 of 33 declared devices.
Catalogue references include 31061, 31063, 31064, 31094, 31095, 41093.
European nomenclature codes declared: Z12011016, Z12011005, Z12011085.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | INTERMEDIC ARFRAN, S.A. (ES) · FDA 3008206114 |
| Devices in EUDAMED | 33 |
| Country of registration | Spain |
Device-level evidence
| Devices with a numeric GTIN | 33 |
|---|---|
| Found in the U.S. device database | 0 |
| Share | 0.0 % |
Canadian market access
| Health Canada licence listing | Licensed in Canada |
|---|---|
| Matched entry | INTERMEDIC ARFRAN S.A. |
What it holds in Canada
| Licences on record | 3 |
|---|---|
| Currently active | 0 |
| Class 3 devices | 3 |
| First licensed | 2005-10-18 |
Licence types: System (2), Device Family (1).
Licensed under: MULTIDIODE ENDO 30 LASER SYSTEM, MULTIDIODE SURGICAL LASER, MULTIDIODE S30 PODYLAS.
North American profile: Both markets. INTERmedic Arfran s.a. is registered in both the United States and Canada.