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Millennium 72-5212576

by Avalign Technologies Inc.

Millennium 72-5212576 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 5 Jan 2022 (UDI-DI 00190776162832), 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 Number00190776162832 UDI-DI Date5 Jan 2022ListedStatusListed 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  • Withdrawn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
Suture knot pusher, reusable
Model / reference
72-5212576
Primary DI / UDI-DI
00190776162832
FDA product code
GCJ
GMDN term
Suture knot pusher, reusable
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Suture knot pusher, reusable

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Other devices filed under Suture knot pusher, reusable.

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)