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Hematology Analyzer

EUDAMED

Class B (EU MDR)

Ref 02-13-04-0010-00Model EXZ 6000Pro, EXZ 6010Pro, EXZ 6020Pro

by Zybio Inc.

Identity

Device Name
Hematology Analyzer EUDAMED
Model / Reference
EXZ 6000Pro, EXZ 6010Pro, EXZ 6020Pro EUDAMED
02-13-04-0010-00 EUDAMED

Identifiers

Primary DI / UDI-DI
06941967200895 EUDAMED
Basic UDI-DI
6973262860003924 EUDAMED
EMDN Code
W0202010101 AUTOMATED WHOLE BLOOD HEMATOLOGY ANALYSERS - LOW ROUTINE (Throughput <= 100 samples/hr) EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

Hematology Analyzer by Zybio Inc. — Class B — 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

Manufacturer
Zybio Inc.
EUDAMED SRN
CN-MF-000003349
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 8e946ddd-69e4-4c11-b8e1-3f2842fd7b98 61 fields · synced Jun 20, 2026