Endoscope connector C1

• FDA 510(k) K854414 decided 12 Mar 1986 Active
• FDA GUDID UDI-DI 03700620600020 listed 7 Nov 2023 Listed

1. 12 Mar 1986 Cleared FDA 510(k) K854414
2. 7 Nov 2023 Listed FDA GUDID 03700620600020

Trade name

Endoscope connector

Generic name

Rigid optical bronchoscope

Model / reference

C1

Primary DI / UDI-DI

03700620600020

510(k) Number

K854414 ↗

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

Category: Rigid optical bronchoscope

Other devices filed under FDA product code EOQ (Bronchoscope (Flexible Or Rigid)).

• DISPOSABLE BIOPSY FORCEPS FB-221D N5431930 by Olympus Medical Systems Corporation
• FLEXIBLE FIBER OPTIC ENDOSCOPE by Optimed Technologies, Inc.
• Flexible 19G EBUS Needle by Spiration, Inc.
• 10101JUA by Karl Storz SE & CO. KG
• OLYMPUS BASKET GRASPERS by Olympus America, Inc.
• DISPOSABLE CYTOLOGY BRUSH BC-202D-1210 by Olympus Medical Systems Corporation
• OLYMPUS FG SERIES OF RAT TOOTH GRASPING FORCEPS (ENT) by Olympus America, Inc.
• MILL-ROSE LARYNGOSCOPIC INJECTION NEEDLE by Mill-Rose Laboratory
• MILL-ROSE PROTECTED TRANSLARYNGOSCOPIC CATHETER by Mill-Rose Laboratory
• PeriFLEX by Spiration, Inc.

• Adult introducer tube BR2000-3

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

• Sterilization basket without lid DJ-4561

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

• Pediatric tube BT2403-3

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

• Pediatric plunger BP2402-3

  Class II

  FDA 510(k) K854414 Active Cleared 12 Mar 1986 GUDID on market

See all devices from Efer Endoscopy →