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Myoglobin (MYO) Kit (Latex Enhanced Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref 01.09.04.02.EC.01

by Zybio Inc.

Identity

Device Name
Myoglobin (MYO) Kit (Latex Enhanced Immunoturbidimetric Method) EUDAMED
Model / Reference
01.09.04.02.EC.01 EUDAMED

Identifiers

Primary DI / UDI-DI
06941967223221 EUDAMED
Basic UDI-DI
B-06941967223221 EUDAMED
EMDN Code
W01021304 MYOGLOBIN EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

Myoglobin (MYO) Kit (Latex Enhanced Immunoturbidimetric Method) by Zybio Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDD

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Manufacturer

Manufacturer
Zybio Inc.
EUDAMED SRN
CN-MF-000003349
Authorised Representative
Lotus NL B.V. NL-AR-000000121

Sources (1)

  • EUDAMED aa5e8e84-3aec-44e1-a97e-76efef659364 61 fields · synced Jul 9, 2026