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Millennium 85-51000213

by Avalign Technologies Inc.

Millennium 85-51000213 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 10 May 2024 (UDI-DI 00190776387686), 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 Number00190776387686 UDI-DI Date10 May 2024ListedStatusListed 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  • Withdrawn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
Surgical bulldog clamp, reusable
Model / reference
85-51000213
Primary DI / UDI-DI
00190776387686
FDA product code
DXC
GMDN term
Surgical bulldog clamp, reusable
Device class
Class II
Regulation number
870.4450
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Surgical bulldog clamp, reusable

Similar devices in this category

Other devices filed under Surgical bulldog clamp, reusable.

Other devices from Avalign Technologies Inc.

See all devices from Avalign Technologies Inc. →

Properties

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