COMEPA INDUSTRIES
FR-MF-000004169 · France · TREMBLAY EN FRANCE
COMEPA INDUSTRIES is registered in the European database on medical devices as a manufacturer, with 12 devices declared. It is also registered as a device establishment with the U.S. FDA.
What this manufacturer declares
| Class IIa | 11 |
|---|---|
| Class IIb | 1 |
Most frequent device types declared: 305200001, 3E6CAUUNS, BLOCLEDF, LPMAC1, LRMIL00.
Among these devices, 4 are declared reusable, 1 active.
Devices declared under this manufacturer
- BLOC DE RECHANGE LED
- CORDON POUR AIGUILLE EEG
- ELECTRODE CUPULE USAGE UNIQUE
- ELECTRODE ECG PREGELIFIEE
- ELECTRODE PRESSION OVALE
- ELECTRODE TENS DIAMETRE 30 MM
- Electrode Neurocom Prégélifié Repositionnable
- LAME DE LARYNGOSCOPE REUTILISABLE
- Lame de Laryngoscope usage unique
- Manche de laryngoscope à LED
- PLACOM
Catalogue references include 305200001, 3E6CAUUNS, HANDLED2, LPMAC1, LRMIL00, T707.
European nomenclature codes declared: Z12021003, N010180, C020501, R9002, N010201, K02010201.
United States market access
| FDA establishment register | Registered with FDA |
|---|---|
| Matched entry | COMEPA INDUSTRIES LIMITED (CN) · FDA 3021602003 |
| Devices in EUDAMED | 12 |
| Country of registration | France |
Device-level evidence
| Devices with a numeric GTIN | 12 |
|---|---|
| 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: United States only. COMEPA INDUSTRIES is registered in the United States but was not found in the Canadian register.