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Pentax Fur-9RBS

by Hoya Corporation

Pentax Fur-9RBS is a Class II device made by Hoya Corporation, listed in FDA GUDID since 7 Apr 2017 (UDI-DI 04961333227839), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number04961333227839 UDI-DI Date7 Apr 2017ListedStatusListed 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  • Withdrawn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
Pentax
Generic name
Flexible fibreoptic ureterorenoscope
Model / reference
FUR-9RBS
Primary DI / UDI-DI
04961333227839
FDA product code
FGB
GMDN term
Flexible fibreoptic ureterorenoscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Related devices

Category: Flexible fibreoptic ureterorenoscope

Other devices from Hoya Corporation

See all devices from Hoya Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (11, all answered No)