Skip to content

Rhythmlink® NCVG50

by Rhythmlink International, LLC

Rhythmlink® NCVG50 is a Class II device made by Rhythmlink International, LLC, listed in FDA GUDID since 30 Jan 2023 (UDI-DI 10816312026495), 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 Number10816312026495 UDI-DI Date30 Jan 2023ListedStatusListed 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  • Withdrawn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
Rhythmlink®
Generic name
Analytical non-scalp cutaneous electrode
Model / reference
NCVG50
Primary DI / UDI-DI
10816312026495
FDA product code
GXY
GMDN term
Analytical non-scalp cutaneous electrode
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution

Related devices

Category: Analytical non-scalp cutaneous electrode

Similar devices in this category

Other devices filed under Analytical non-scalp cutaneous electrode.

Other devices from Rhythmlink International, LLC

See all devices from Rhythmlink International, LLC →

Properties

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