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vMap Disposables VMDISP3

by Vektor Medical, Inc.

vMap Disposables VMDISP3 is a Class II device made by Vektor Medical, Inc., listed in FDA GUDID since 8 May 2026 (UDI-DI 00860007954146), registry data as of 22 Oct 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00860007954146 UDI-DI Date8 May 2026ListedStatusListed 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  • Withdrawn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
vMap Disposables
Generic name
Cardiac mapping system workstation
Model / reference
VMDISP3
Primary DI / UDI-DI
00860007954146
FDA product code
DQK
GMDN term
Cardiac mapping system workstation
Device class
Class II
Regulation number
870.1425
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code DQK (Computer, Diagnostic, Programmable).

Other devices from Vektor Medical, Inc.

See all devices from Vektor Medical, Inc. →

Properties

  • Single use
  • Convenience kit
  • Lot / batch number
Other properties (12, all answered No)