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Rhythmlink® DC29152

by Rhythmlink International, LLC

Rhythmlink® DC29152 is a Class II device made by Rhythmlink International, LLC, listed in FDA GUDID since 27 Oct 2026 (UDI-DI 10816312029427), registry data as of 9 Nov 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 9 Nov 2026.

Regulatory status

as of registry sync 9 Nov 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10816312029427 UDI-DI Date27 Oct 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  • Withdrawn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
Rhythmlink®
Generic name
Analytical scalp electrode, single-use
Model / reference
DC29152
Primary DI / UDI-DI
10816312029427
FDA product code
GXY
GMDN term
Analytical scalp electrode, single-use
Device class
Class II
Regulation number
882.1320
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GXY (Electrode, Cutaneous).

Other devices from Rhythmlink International, LLC

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Properties

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