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Br-923DA

by Nihon Kohden America, Inc.

Br-923DA is a Class II device made by Nihon Kohden America, Inc., listed in FDA GUDID since 19 Sep 2016 (UDI-DI 00841983100192), registry data as of 22 Oct 2026.

Listed FDA GUDID listing, not in commercial distribution

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 Number00841983100192 UDI-DI Date19 Sep 2016ListedStatusListed GUDID: not 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  • Withdrawn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

Generic name
Electrocardiographic lead set, reusable
Model / Ref / Catalog
BR-923DA
Primary DI / UDI-DI
00841983100192
FDA product code
DPS
GMDN term
Electrocardiographic lead set, reusable
Device class
Class II
Regulation number
870.2340
GUDID distribution status
Not in Commercial Distribution

Other devices from Nihon Kohden America, Inc.

See all devices from Nihon Kohden America, Inc. →

Properties

  • Prescription use
  • Lot / batch number
Other properties (13, all answered No)