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Apolipoprotein A1 (Apo A1) Kit (Immunoturbidimetric Method)

EUDAMED

Class IVD General (EU MDR)

Ref 01.09.02.06.EC.01

by Zybio Inc.

Identity

Device Name
Apolipoprotein A1 (Apo A1) Kit (Immunoturbidimetric Method) EUDAMED
Model / Reference
01.09.02.06.EC.01 EUDAMED

Identifiers

Primary DI / UDI-DI
06941967204367 EUDAMED
Basic UDI-DI
B-06941967204367 EUDAMED
EMDN Code
W0102010401 APOLIPOPROTEIN A I EUDAMED

Classification

Device Class
Class IVD General EUDAMED
Market of Registration
Germany 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

Category: Apolipoprotein A-I (Apo A1) IVD, reagent

Apolipoprotein A1 (Apo A1) Kit (Immunoturbidimetric Method) by Zybio Inc. — Class IVD General — IVDD — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Apolipoprotein A-I (Apo A1) IVD, reagent.

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 0f19203f-b0c1-4470-bd6c-e3f6a7c5d57f 61 fields · synced Jul 9, 2026