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Millennium 72-420598

by Avalign Technologies Inc.

Millennium 72-420598 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 2 Nov 2021 (UDI-DI 00190776189112), 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 Number00190776189112 UDI-DI Date2 Nov 2021ListedStatusListed 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  • Withdrawn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 laryngopharyngoscope
Model / reference
72-420598
Primary DI / UDI-DI
00190776189112
FDA product code
CCW
GMDN term
Rigid optical laryngopharyngoscope
Device class
Class I
Regulation number
868.5540
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Rigid optical laryngopharyngoscope

Similar devices in this category

Other devices filed under Rigid optical laryngopharyngoscope.

Other devices from Avalign Technologies Inc.

See all devices from Avalign Technologies Inc. →

Properties

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