Skip to content

V. Mueller AU12314

by Steris Corporation

V. Mueller AU12314 is a Class I device made by Steris Corporation, listed in FDA GUDID since 13 Jul 2018 (UDI-DI 10885403009860), 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 Number10885403009860 UDI-DI Date13 Jul 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  • Withdrawn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
Middle ear chisel
Model / Ref / Catalog
AU12314
Primary DI / UDI-DI
10885403009860
FDA product code
JYT
GMDN term
Middle ear chisel
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Middle ear chisel

Similar devices in this category

Other devices filed under Middle ear chisel.

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)