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V. Mueller LA6476

by Steris Corporation

V. Mueller LA6476 is a Class II device made by Steris Corporation, listed in FDA GUDID since 4 Oct 2016 (UDI-DI 10885403052415), 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 Number10885403052415 UDI-DI Date4 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  • Withdrawn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
V. Mueller
Generic name
Electrosurgical handpiece, reusable
Model / Ref / Catalog
LA6476
Primary DI / UDI-DI
10885403052415
FDA product code
GEI
GMDN term
Electrosurgical handpiece, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Electrosurgical handpiece, reusable

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Other devices filed under Electrosurgical handpiece, reusable.

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Properties

  • Sterilise before use
  • Prescription use
  • Lot / batch number
Other properties (12, all answered No)