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GeneMind

EUDAMED

Class A (EU MDR)

Ref S000499Model S-1 FCL-D 100-D,S-1 FCL 100,S-1 FCL 300,S-1 FCM-D 100-D,S-1 FCM 100,S-1 FCM 300

by GeneMind Biosciences Co., Ltd.

Identity

Trade Name
GeneMind EUDAMED
Device Name
FASTASeq S Dx Universal Reaction Kit for Sequencing EUDAMED
Model / Reference
S-1 FCL-D 100-D,S-1 FCL 100,S-1 FCL 300,S-1 FCM-D 100-D,S-1 FCM 100,S-1 FCM 300 EUDAMED
S000499 EUDAMED

Identifiers

Primary DI / UDI-DI
06974968583896 EUDAMED
Basic UDI-DI
697496858BZ01UU EUDAMED
Direct Marketing DI
06974968583896 EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Türkiye 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

GeneMind by GeneMind Biosciences Co., Ltd. — 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
CN-MF-000025785
Authorised Representative
Umedwings Netherlands B.V. NL-AR-000000444

Sources (1)

  • EUDAMED 4826c4e0-83fa-4572-8466-e86c129ef4e0 61 fields · synced Jun 18, 2026