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V. Mueller MO2170

by Steris Corporation

V. Mueller MO2170 is a Class I device made by Steris Corporation, listed in FDA GUDID since 6 Feb 2019 (UDI-DI 10885403059186), 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 Number10885403059186 UDI-DI Date6 Feb 2019ListedStatusListed 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  • Withdrawn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
ENT soft-tissue cutting forceps
Model / Ref / Catalog
MO2170
Primary DI / UDI-DI
10885403059186
FDA product code
KBT
GMDN term
ENT soft-tissue cutting forceps
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: ENT soft-tissue cutting forceps

Similar devices in this category

Other devices filed under ENT soft-tissue cutting forceps.

Other devices from Steris Corporation

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Properties

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