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Vektor Medical vMap Software vMap Software - US

by Vektor Medical, Inc.

Vektor Medical vMap Software vMap Software - US is a Class II device made by Vektor Medical, Inc., listed in FDA GUDID since 8 May 2026 (UDI-DI 00199874185187), registry data as of 23 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 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00199874185187 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  • Withdrawn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
Vektor Medical vMap Software
Generic name
Cardiac mapping system workstation
Model / reference
vMap Software - US
Primary DI / UDI-DI
00199874185187
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).

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Properties

  • Convenience kit
Other properties (14, all answered No)