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VERIFY Bowie Dick

by Albert Browne, Ltd. United States EUDAMEDGUDID

Ref EQC009Model Bowie Dick Test Pack Product code JOJEMDN Z12011385

Regulatory status

as of 25 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR EUDAMED Number0724995LCPENBOWIEDICK23 Basic UDI-DIDate6 Aug 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00724995362973 UDI-DIDate16 Jul 2026ListedStatusIn distribution

Coverage

2 jurisdictions

United States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaUnited States of AmericaSwedenFinlandFinlandSwedenFinlandFinlandSwedenSwedenLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyGermanyPolandPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaPolandFranceFranceAustriaHungaryRomaniaFranceFranceSloveniaBulgariaPortugalSpainSpainItalySpainSpainCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not known
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Certificates: none listed in EUDAMED

Recalls

1 recall · FDA

    • Terminated Z-1736-2022 FDA Class III initiated 10 Aug 2022

    Product contains incorrect chemical indicators in packaging.

Specification

EUDAMED · GUDID · synced 24 Oct 2026

Trade Name
Verify
Generic Name
Chemical/physical sterilization process indicator
Model / Ref / Catalog
Bowie Dick Test Pack, EQC009, Bowie Dick
Primary DI / UDI-DI
00724995362973
Basic UDI-DI
0724995LCPENBOWIEDICK23
510(k) Number
FDA Product Code
JOJ
EMDN Code
Z12011385 Cleaning, disinfection and sterilisation instruments - consumables
GMDN Term
Chemical/physical sterilization process indicator
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
880.2800
Market of Registration
Ireland
Commercial Distribution
In Commercial Distribution

Truth per registry

2 sources · 2 fields differ

FieldEUDAMEDGUDID
Model / ReferenceEUDAMED
Bowie Dick Test Pack
EQC009
GUDID
Bowie Dick
Device ClassEUDAMED
Class I
GUDID
Class II

Related devices

Cleared under the same submission (K002741)

Cleared under the same submission (K162758)

Show all (12)

Other devices from Albert Browne, Ltd.

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Properties & raw data

Show properties, registry sources and raw records
  • Single Use
  • Over-the-Counter
  • Lot / Batch Number
  • Expiration Date
Other properties (20)
  • Sterile: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No
  • Serial Number: No
  • Manufacturing Date: No

Sources (2)

  • FDA UDI 7ef7b0d4-f942-4752-9138-56077060ef13 37 fields · synced 24 Oct 2026
  • EUDAMED 00724995362973|0724995LCPENBOWIEDICK23 61 fields · synced 24 Oct 2026