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Millennium 72-385020

by Avalign Technologies Inc.

Millennium 72-385020 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 11 Jul 2025 (UDI-DI 00190776405045), 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 Number00190776405045 UDI-DI Date11 Jul 2025ListedStatusListed 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  • Withdrawn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
ENT surgical procedure kit, non-medicated, reusable
Model / reference
72-385020
Primary DI / UDI-DI
00190776405045
FDA product code
LRC
GMDN term
ENT surgical procedure kit, non-medicated, reusable
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 surgical procedure kit, non-medicated, reusable

Other devices from Avalign Technologies Inc.

See all devices from Avalign Technologies Inc. →

Properties

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