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Millennium AE SR551R

by Avalign Technologies Inc.

Millennium AE SR551R is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 22 May 2017 (UDI-DI 00190776083731), 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 Number00190776083731 UDI-DI Date22 May 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  • Withdrawn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
AE SR551R
Primary DI / UDI-DI
00190776083731
FDA product code
GEI
GMDN term
General-purpose endoscopic needle, reusable
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

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.

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Properties

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