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V. Mueller SU10810120

by Steris Corporation

V. Mueller SU10810120 is an open-surgery stone-retrieval forceps (FDA Class I; FDA product code FGM, Probe and Director, Gastro-Urology) made by Steris Corporation, listed in FDA GUDID since 17 Sep 2018 (UDI-DI 10885403061332), 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 Number10885403061332 UDI-DI Date17 Sep 2018ListedStatusListed 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  • Withdrawn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
V. Mueller
Generic name
Open-surgery stone-retrieval forceps
Model / Ref / Catalog
SU10810120
Primary DI / UDI-DI
10885403061332
FDA product code
FGM
GMDN term
Open-surgery stone-retrieval forceps
Device class
Class I
Regulation number
876.4730
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Open-surgery stone-retrieval forceps

Similar devices

Other devices filed under FDA product code FGM (PROBE AND DIRECTOR, GASTRO-UROLOGY).

Other devices from Steris Corporation

See all devices from Steris Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)