Skip to content

Millennium 9-1001

by Avalign Technologies Inc.

Millennium 9-1001 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 13 Nov 2023 (UDI-DI 00190776322199), 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 Number00190776322199 UDI-DI Date13 Nov 2023ListedStatusListed 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  • Withdrawn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
Nasal speculum, reusable
Model / reference
9-1001
Primary DI / UDI-DI
00190776322199
FDA product code
EPY
GMDN term
Nasal speculum, reusable
Device class
Class I
Regulation number
878.1800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Nasal speculum, 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)