Skip to content

Millennium LI-480

by Avalign Technologies Inc.

Millennium LI-480 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 11 Sep 2017 (UDI-DI 00190776118594), 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 Number00190776118594 UDI-DI Date11 Sep 2017ListedStatusListed 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  • Withdrawn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
General-purpose endoscopic needle, reusable
Model / reference
LI-480
Primary DI / UDI-DI
00190776118594
FDA product code
GDM
GMDN term
General-purpose endoscopic needle, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization
Size
Needle Gauge — 14 Gauge

Related devices

Category: General-purpose endoscopic needle, reusable

Similar devices in this category

Other devices filed under General-purpose endoscopic needle, reusable.

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)