Efer Endoscopy
Country not established
Efer Endoscopy is a medical device manufacturer, with 90 devices listed in FDA GUDID and EUDAMED (FDA Class II) as of 14 Nov 2026.
- Devices
- 90
Registry facts
- Registries
- FDA GUDID 90
- EUDAMED 1
- Device classes
- FDA Class II 90
- Sites and related companies
- Efer Endoscopy France
- Identifiers
- DUNS 286097451
What Efer Endoscopy makes
EFER Endoscopy manufactures rigid optical bronchoscopes and associated accessories, including introducer tubes for both adult and pediatric use, plunger mechanisms, sterilization baskets, and biopsy forceps. Their portfolio also covers base units—compact and adult-sized—as well as silicone caps and bronchial endoscopes designed for airway visualization and procedural support.
The company’s devices are classified as Class II under FDA regulations and are listed in the FDA’s Unique Device Identifier (UDI) database. Their products are developed and distributed from the United States.
Catalogue
Search and filter all 90 devicesShowing 1-50 of 90
Company details
- DUNS number
- 286097451
Sites
- Efer Endoscopy FRFEI 3006493107 0 devices
Frequently asked questions
How many devices does EFER ENDOSCOPY have in the registry?
The registry currently lists 90 devices for EFER ENDOSCOPY. Devices recorded under merged duplicate company entries are counted once.
Which registries list EFER ENDOSCOPY's devices?
Among its 50 most recently registered devices, EFER ENDOSCOPY has devices listed in FDA GUDID (50 devices).
What risk classes do EFER ENDOSCOPY's devices fall under?
Among its 50 most recently registered devices, the classes recorded for EFER ENDOSCOPY's devices are Class II. Each device page shows its own class and authorisation.
What are the newest devices from EFER ENDOSCOPY in the registry?
The most recently registered devices listed for EFER ENDOSCOPY include Adult introducer tube BR2000-3, Sterilization basket without lid DJ-4561, Pediatric tube BT2403-3 and Pediatric plunger BP2402-3.