10317LR
10317LR is a Class II device made by Karl Storz SE & CO. KG, listed in FDA GUDID since 23 Sep 2016 (UDI-DI 04048551045602), registry data as of 22 Oct 2026.
Listed
Valid until
Not applicable
FDA recalls
Not checked
Documents
None
Trust
Regulatory status
| Region | Authorization | Number | Date | Status |
|---|---|---|---|---|
| United States | GUDID listing | Number04048551045602 | Date23 Sep 2016 | StatusListed |
Official records
- AccessGUDID record 04048551045602
Coverage
- Active
- Expiring
- Withdrawn
- Listed
- Not covered
United States — GUDID listing Listed
Specification
- Generic name
- Rigid optical bronchoscope
- Model / reference
- 10317LR
- Primary DI / UDI-DI
- 04048551045602
- FDA product code
- EOQ
- GMDN term
- Rigid optical bronchoscope
- Device class
- Class II
- Regulation number
- 874.4680
- GUDID distribution status
- In Commercial Distribution
- Sterilisation method
- Moist Heat or Steam Sterilization
Similar devices
Other devices filed under FDA product code EOQ (BRONCHOSCOPE (FLEXIBLE OR RIGID)).
- Single Use Grasping Forceps FG-214P, Single Use Grasping Forceps FG-220P, Single Use Grasping Forceps FG-226C, Single Use Grasping Forceps FG-232L, Single Use Grasping Forceps FG-804L by Olympus Medical Systems Corporation
- EVIS EXERA III Bronchovideoscope Olympus BF-XP190, EVIS EXERA III Bronchovideoscope Olympus BF-P190 by Olympus Medical Systems Corporation
- Neo-Bronchoscope -Digital Video Bronchoscopy System(Rigid/Flexible) by Prosurg, Inc
- Ion 380707 by Intuitive Surgical, Inc.
- BF 240/P240/IT240 BRONCHOVIDEOSCOPE & ACCESSORIES by Olympus America, Inc.
- Auris Robotic Endoscopy System (ARES) by Auris Surgical Robotics, Inc.
- Ion 490206 by Intuitive Surgical, Inc.
- RITE-BITE BIOPSY FORCEPS by Mill-Rose Laboratory
- OLYMPUS FB SERIES BIOPSY FORCEPS by Olympus America, Inc.
- FUJIFILM Bronchoscope by FUJIFILM CORPORATION