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Continuous ECG Platform VV330

by VivaLNK, Inc.

Continuous ECG Platform VV330 is a Class II device made by VivaLNK, Inc., listed in FDA GUDID since 30 Jan 2020 (UDI-DI 00865064000157), 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 Number00865064000157 UDI-DI Date30 Jan 2020ListedStatusListed 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  • Withdrawn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
Continuous ECG Platform
Generic name
Electrocardiography telemetric monitoring system
Model / reference
VV330
Primary DI / UDI-DI
00865064000157
FDA product code
DRG
GMDN term
Electrocardiography telemetric monitoring system
Device class
Class II
Regulation number
870.2910
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Similar devices

Other devices filed under FDA product code DRG (Transmitters And Receivers, Physiological Signal, Radiofrequency).

Other devices from VivaLNK, Inc.

See all devices from VivaLNK, Inc. →

Properties

  • Prescription use
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (11, all answered No)