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Millennium 1-350150

by Avalign Technologies Inc.

Millennium 1-350150 is a Class I device made by Avalign Technologies Inc., listed in FDA GUDID since 1 Nov 2021 (UDI-DI 00190776166519), 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 Number00190776166519 UDI-DI Date1 Nov 2021ListedStatusListed 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  • Withdrawn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
Telemetric sphygmomanometer
Model / reference
1-350150
Primary DI / UDI-DI
00190776166519
FDA product code
GAD
GMDN term
Telemetric sphygmomanometer
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Telemetric sphygmomanometer

Similar devices

Also classified as Telemetric sphygmomanometer.

Similar devices

Other devices filed under FDA product code GAD (RETRACTOR).

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)