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Diazyme DZ568A-CA5

by Diazyme Laboratories, Inc.

Ref DZ568A-CA5

Diazyme DZ568A-CA5 is a device classified as Class B in the EU and Class II in the US made by Diazyme Laboratories, Inc., registered in EUDAMED on 25 Sep 2026 (Basic UDI-DI 0817089021464XF), cleared under FDA 510(k) K071971 on 17 Sep 2007 and listed in FDA GUDID since 21 Jul 2020 (UDI-DI 00817089021464), active as of 22 Oct 2026.

Active European Union and United States. Also listed in GUDID (US).

CE IVDR 510(k)

Valid until

No date given

CE: no date in EUDAMED. FDA: not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

510(k) K071971

FDA submission, from GUDID

Trust

Unverified

Source EUDAMED, GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/IVDR EUDAMED Number0817089021464XF Basic UDI-DI 00817089021464UDI-DIDate25 Sep 2026RegisteredStatusActive
United StatesGUDID listing GUDID Number00817089021464 UDI-DI Date21 Jul 2020ListedStatusListed GUDID: in commercial distribution
United StatesFDA 510(k)SESE GUDID from GUDID Substantially Equivalent · Special NumberK071971 Date17 Sep 2007DecidedStatusActive

Official records

Across registries

3 registries list this device

  • EUDAMED Basic UDI-DI 0817089021464XF registered 25 Sep 2026 Active
  • FDA 510(k) K071971 decided 17 Sep 2007 Active
  • FDA GUDID UDI-DI 00817089021464 listed 21 Jul 2020 Listed

Timeline

3 dated events

  1. Cleared FDA 510(k) K071971
  2. Listed FDA GUDID 00817089021464
  3. Registered EUDAMED 0817089021464XF

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/IVDR Active
  • United States FDA 510(k) Active

Specification

EUDAMED · GUDID

Trade name
Diazyme Homocysteine Enzymatic 5-Point Calibrator Set EUDAMED
Diazyme GUDID
Generic name
Homocysteine IVD, calibrator
Device name
Diazyme Homocysteine Enzymatic Calibrators
Model / reference
DZ568A-CA5
Primary DI / UDI-DI
00817089021464
Basic UDI-DI
0817089021464XF
510(k) Number
FDA product code
JIX, LPS
EMDN code
W0102152204 Cardiac marker standards and calibrators
GMDN term
Homocysteine IVD, calibrator
Device class
Class B EUDAMED
Class II GUDID
Regulation number
862.1150, 862.1377
EU registration type
Standard device
EU market of registration
Germany
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device classEUDAMED
Class B
GUDID
Class II

Device class is stated on each registry's own scale: Class B in the EU (EUDAMED), Class II in the US (FDA GUDID). EU and US classes are different schemes, so this is not a disagreement.

Related devices

Category: Homocysteine IVD, calibrator

Cleared under the same submission (K071971)

Similar devices in this category

Other devices filed under CARDIAC MARKER STANDARDS AND CALIBRATORS.

Other devices from Diazyme Laboratories, Inc.

See all devices from Diazyme Laboratories, Inc. →

Properties

  • Contains human tissues or cells
  • Professional testing
  • Convenience kit
  • Lot / batch number
  • Expiration date
Other properties (21, all answered No)