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Diluent

EUDAMED

Class A (EU MDR)

Ref 8-866Ref 8-879Ref 8-882Ref 8-886

by PZ CORMAY Spółka Akcyjna

Identity

Trade Name
DILUENT EUDAMED
Device Name
DILUENT EUDAMED
Model / Reference
8-866 EUDAMED
8-879 EUDAMED
8-882 EUDAMED
8-886 EUDAMED

Identifiers

Primary DI / UDI-DI
05907514688661 EUDAMED
05907514688791 EUDAMED
05907514688821 EUDAMED
05907514688869 EUDAMED
Basic UDI-DI
590751468-866_8-886CR EUDAMED
EMDN Code
W0103010105 CBC-REAGENTS (CLEANING-/DILUTING-/LYSING-/SHEATH-FLUIDS) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Poland EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Diluent by PZ CORMAY Spółka Akcyjna — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
PL-MF-000023053

Sources (4)

  • EUDAMED 2db8a317-b983-4509-a6a8-2aaa24fb0463 61 fields · synced Oct 6, 2026
  • EUDAMED 3881f9a3-44aa-4328-8de7-8f631a26f525 61 fields · synced May 17, 2026
  • EUDAMED 60f0ce51-a80e-4322-b521-21043a340c5a 61 fields · synced May 17, 2026
  • EUDAMED d9a22ebd-142d-4cf1-9177-6ccfdf967ff5 61 fields · synced May 18, 2026