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Sign in to claim this brandEFER ENDOSCOPY
US
Last updated May 23, 2026
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.
Written from this company's registered devices by an AI model, and not verified by a human reviewer.
Frequently asked questions
What types of medical devices does EFER Endoscopy manufacture?
EFER Endoscopy specializes in rigid optical bronchoscopes, which are used for visualizing the airways. Their product portfolio also includes related accessories such as adult and pediatric introducer tubes, plunger mechanisms, sterilization baskets, optical biopsy forceps, base units (compact and adult-sized), silicone caps, and bronchial endoscopes. These devices support airway visualization and procedural interventions in medical settings.
Where is EFER Endoscopy based, and where are their devices developed and distributed?
EFER Endoscopy is based in the United States. Their devices are developed and distributed from there, ensuring compliance with U.S. regulatory standards and quality controls.
Which regulatory registries list EFER Endoscopy’s devices?
EFER Endoscopy’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry helps track and identify medical devices authorized for use in the U.S., ensuring transparency and traceability in the healthcare supply chain.
How are EFER Endoscopy’s devices classified under FDA regulations?
EFER Endoscopy’s devices fall under Class II classification according to FDA regulations. This classification typically applies to devices that pose moderate risk and require special controls beyond general controls to ensure safety and effectiveness, such as bronchoscopes and associated accessories.
AI-generated from registry data and not verified by a human reviewer.
Information
- Country
- US
- Address
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- Website
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- Phone
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- PRRC Contact
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- EUDAMED SRN
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- FDA FEI Number
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- DUNS Number
- 286097451
Catalogue (90)
Page 2 of 2| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| Pediatric loader | BI2402-3 | FDA UDI | Class II | Active |
| Adult plunger tube | BP2000-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2317-3 | FDA UDI | Class II | Active |
| Adult plunger tube | BP2101-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2302-3 | FDA UDI | Class II | Active |
| Jumbo plunger tube | BP2701-3 | FDA UDI | Class II | Active |
| Jumbo loader | BI2701-3 | FDA UDI | Class II | Active |
| Lid for sterilization basket | DJ-4886 | FDA UDI | Class II | Active |
| Silicone cap | BS2102-3 | FDA UDI | Class II | Active |
| Adult bronchial tube | BT2106-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2304-3 | FDA UDI | Class II | Active |
| Adult bronchial tube | BT2000-3 | FDA UDI | Class II | Active |
| Lateral obturator | BB2401-3 | FDA UDI | Class II | Active |
| Endoscope connector | C4 | FDA UDI | Class II | Active |
| Luer Rongeur forceps | 411-548 | FDA UDI | Class II | Active |
| Endoscope connector | C2 | FDA UDI | Class II | Active |
| Pediatric tube | BT2404-3 | FDA UDI | Class II | Active |
| Adult bronchial tube | BT2101-3 | FDA UDI | Class II | Active |
| Adult tracheal tube | BT2205-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2307-3 | FDA UDI | Class II | Active |
| Adult tracheal tube | BT2203-3 | FDA UDI | Class II | Active |
| Adult loader | BI2101-3 | FDA UDI | Class II | Active |
| Adult loader | BI2103-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2309-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2319-3 | FDA UDI | Class II | Active |
| Optical stent removal forceps | 32-3230-430HM-SA | FDA UDI | Class II | Active |
| Adult bronchial tube | BT2103-3 | FDA UDI | Class II | Active |
| Sterilzation basket with lid | DJ-4046-SPEC | FDA UDI | Class II | Active |
| Silicone mat | DJ-4929 | FDA UDI | Class II | Active |
| Adult introducer tube | BR2200-3 | FDA UDI | Class II | Active |
| Adult loader | BI2001-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2318-3 | FDA UDI | Class II | Active |
| Adult bronchial tube | BT2105-3 | FDA UDI | Class II | Active |
| Jumbo bronchoscope tube | BT2603-3 | FDA UDI | Class II | Active |
| Sterilization basket without lid | DJ-4561-SPEC | FDA UDI | Class II | Active |
| Adult introducer tube | BR2103-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2300-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2306-3 | FDA UDI | Class II | Active |
| Jumbo introducer tube | BR2701-3 | FDA UDI | Class II | Active |
| Silicone cap | BS2310-3 | FDA UDI | Class II | Active |
Related Companies
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FDA Establishments (1)
Establishments registered with the FDA under this company group, matched by name.
- Efer Endoscopy LA CIOTAT Bouches-du-Rhone · FR FEI 3006493107