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VICTOR2 D 1420-021

by Wallac Oy

VICTOR2 D 1420-021 is a Class I device made by Wallac Oy, listed in FDA GUDID since 19 Mar 2019 (UDI-DI 06438147121373), not in commercial distribution (GUDID) as of 12 Nov 2026.

Listed FDA GUDID listing, not in commercial distribution

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 12 Nov 2026.

Regulatory status

as of registry sync 12 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number06438147121373 UDI-DI Date19 Mar 2019ListedStatusListed GUDID: not 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  • Withdrawn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
VICTOR2 D
Generic name
Fluorescent immunoassay analyser IVD, laboratory
Model / Ref / Catalog
1420-021
Primary DI / UDI-DI
06438147121373
FDA product code
KHO
GMDN term
Fluorescent immunoassay analyser IVD, laboratory
Device class
Class I
Regulation number
862.2560
GUDID distribution status
Not in Commercial Distribution

Similar devices

Other devices filed under FDA product code KHO (Fluorometer, For Clinical Use).

Other devices from Wallac Oy

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Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)