Silicone cap BS2311-3

• FDA 510(k) K854414 decided 12 Mar 1986 Active
• FDA GUDID UDI-DI 03700620600112 listed 7 Nov 2023 Listed

1. 12 Mar 1986 Cleared FDA 510(k) K854414
2. 7 Nov 2023 Listed FDA GUDID 03700620600112

Trade name

Silicone cap

Generic name

Rigid optical bronchoscope

Model / reference

BS2311-3

Primary DI / UDI-DI

03700620600112

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)).

• FUJIFILM Endoscope Model EB-710P; FUJIFILM Processor EP-8000 by FUJIFILM CORPORATION
• COAGULATION ELECTRODE, MODEL 2000; RADIOFREQUENCY GENERATOR, MODEL 20-115 by Broncus Technologies, Inc.
• 10315N by Karl Storz SE & CO. KG
• PENTAX Medical Video Bronchoscope EB-J10 Series by PENTAX of America Inc.
• FUJIFILM Endoscope Model EB-710XT by FUJIFILM Healthcare Americas Corporation
• ENK FIBEROPTIC ATOMIZER SET by Cook, Inc.
• MiiS Horus scope 5007 by Medimaging Integrated Solution, Inc (Miis)
• TBAN by Boston Scientific
• Ion Endoluminal System (IF1000) by Intuitive Surgical, Inc.
• VB-1830/VB-1530, VIDEO BRONCHOSCOPE by Pentax Precision Instrument Corp.

• 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 →