Industrie Celtex S.p.A.
IT-MF-000027968 · Italy · Montecarlo
Industrie Celtex S.p.A. is registered in the European database on medical devices as a manufacturer, with 62 devices declared. It was not found in the U.S. FDA device establishment register.
What this manufacturer declares
| Class IIa | 62 |
|---|
Most frequent device types declared: C62655.
Devices declared under this manufacturer
- ABSOLUTE MT 150 H 50
- BLUENET FIVE MT 50 H 50
- CEL 75 MT 48 H 39
- E-MIX 50 H50
- G7 5050 - SERVOPRAX MEDILUX FIVE MT 50 H 50
- G7 5050 - SERVOPRAX MT 50 H 50
- G7 5055 - SERVOPRAX MEDILUX FIVE.5 MT 50 H 55
- G7 5055 - SERVOPRAX MT 50 H 55
- K7 40 - SERVOPRAX MT 150 H 39
- K7 45 - SERVOPRAX MT 150 H 46
- K7 50 - SERVOPRAX MT 150 H 50
- MEDILUX FIVE MT 50 H 50
Showing 12 of 62 declared devices.
Catalogue references include 60204, 61250-H1, 62607-28, 62655-H1, 62656-H1, 64625.
European nomenclature codes declared: T030502.
United States market access
| FDA establishment register | Not found in the FDA register |
|---|---|
| Devices in EUDAMED | 62 |
| Country of registration | Italy |
⚠️ Not found is not the same as not sold — how this comparison can be wrong.
Device-level evidence
| Devices with a numeric GTIN | 62 |
|---|---|
| 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. Industrie Celtex S.p.A. was not found in either the U.S. or the Canadian register.