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Millennium 72-3140057

by Avalign Technologies Inc.

Millennium 72-3140057 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 1 Aug 2019 (UDI-DI 00190776143787), registry data as of 8 Nov 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 8 Nov 2026.

Regulatory status

as of registry sync 8 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00190776143787 UDI-DI Date1 Aug 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  • Withdrawn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
Millennium
Generic name
Rigid optical cystourethroscope
Model / reference
72-3140057
Primary DI / UDI-DI
00190776143787
FDA product code
GCJ
GMDN term
Rigid optical cystourethroscope
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid optical cystourethroscope

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Other devices filed under Rigid optical cystourethroscope.

Other devices from Avalign Technologies Inc.

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Properties

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