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Avalign VM85-6671

by Avalign Technologies Inc.

Avalign VM85-6671 is a Class II device made by Avalign Technologies Inc., listed in FDA GUDID since 16 Jan 2018 (UDI-DI 00190776124717), 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 Number00190776124717 UDI-DI Date16 Jan 2018ListedStatusListed 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  • Withdrawn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
Avalign
Generic name
Suction cannula, reusable
Model / reference
VM85-6671
Primary DI / UDI-DI
00190776124717
FDA product code
JOL
GMDN term
Suction cannula, reusable
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Suction cannula, reusable

Similar devices in this category

Other devices filed under Suction cannula, 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)