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732607611

by Richard Wolf GmbH

732607611 is a Class II device made by Richard Wolf GmbH, listed in FDA GUDID since 21 Jul 2017 (UDI-DI 04055207057599), 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 Number04055207057599 UDI-DI Date21 Jul 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  • Withdrawn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

Generic name
Flexible fibreoptic ureterorenoscope
Model / Ref / Catalog
732607611
Primary DI / UDI-DI
04055207057599
FDA product code
FAJ
GMDN term
Flexible fibreoptic ureterorenoscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Hydrogen Peroxide

Related devices

Category: Flexible fibreoptic ureterorenoscope

Similar devices in this category

Other devices filed under Flexible fibreoptic ureterorenoscope.

Other devices from Richard Wolf GmbH

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Properties

  • Sterilise before use
  • Manufacturing date
Other properties (13, all answered No)