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Lyse

EUDAMED

Class A (EU MDR)

Ref 01.09.31.03.02.02Model H56 LD-I

by Zybio Inc.

Identity

Device Name
Lyse EUDAMED
Model / Reference
H56 LD-I EUDAMED
01.09.31.03.02.02 EUDAMED

Identifiers

Primary DI / UDI-DI
06941967224594 EUDAMED
Basic UDI-DI
6973262860005828 EUDAMED
EMDN Code
W01030199 HAEMATOLOGY REAGENTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

Lyse by Zybio Inc. — 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

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

Sources (1)

  • EUDAMED 70bcf310-d736-4553-9d74-b594207b372d 61 fields · synced Jun 19, 2026