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Reference Electrode RD-945389D

by DIAMOND DIAGNOSTICS Inc

Reference Electrode RD-945389D is a device made by DIAMOND DIAGNOSTICS Inc, listed in FDA GUDID since 9 Jun 2023 (UDI-DI 00811403017713), 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 Number00811403017713 UDI-DI Date9 Jun 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  • Withdrawn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
Reference Electrode
Generic name
Reference electrode IVD
Model / reference
RD-945389D
Primary DI / UDI-DI
00811403017713
GMDN term
Reference electrode IVD
GUDID distribution status
In Commercial Distribution

Related devices

Category: Reference electrode IVD

Other devices from DIAMOND DIAGNOSTICS Inc

See all devices from DIAMOND DIAGNOSTICS Inc →

Properties

  • Single use
  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Serial number
  • Expiration date
Other properties (8, all answered No)