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Fujifilm Ca-500B

by Fujifilm Corporation

Fujifilm Ca-500B is a Class I device made by Fujifilm Corporation, listed in FDA GUDID since 18 Oct 2016 (UDI-DI 04547410079197), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04547410079197 UDI-DI Date18 Oct 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Fujifilm
Generic name
Flexible video bronchoscope, reusable
Model / reference
CA-500B
Description
This product is the cleaning adapter used in combination with our endoscopes in medical facilities. Do not use this product for any other purpose.
Primary DI / UDI-DI
04547410079197
FDA product code
FCL
GMDN term
Flexible video bronchoscope, reusable
Device class
Class I
Regulation number
876.1075
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible video bronchoscope, reusable

Similar devices in this category

Other devices filed under Flexible video bronchoscope, reusable.

Other devices from Fujifilm Corporation

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Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Manufacturing date
Other properties (10, all answered No)