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BUN Reagent BK-472482D

by DIAMOND DIAGNOSTICS Inc

BUN Reagent BK-472482D is a device made by DIAMOND DIAGNOSTICS Inc, listed in FDA GUDID since 12 Jun 2023 (UDI-DI 00811403011650), 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 Number00811403011650 UDI-DI Date12 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  • Withdrawn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
BUN Reagent
Generic name
Urea IVD, kit, enzyme spectrophotometry
Model / reference
BK-472482D
Primary DI / UDI-DI
00811403011650
GMDN term
Urea IVD, kit, enzyme spectrophotometry
GUDID distribution status
In Commercial Distribution

Related devices

Category: Urea IVD, kit, enzyme spectrophotometry

Other devices from DIAMOND DIAGNOSTICS Inc

See all devices from DIAMOND DIAGNOSTICS Inc →

Properties

  • Prescription use
  • Convenience kit
  • Premarket exempt
  • Lot / batch number
  • Expiration date
  • Manufacturing date
Other properties (9, all answered No)