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GeneMind

EUDAMED

Class A (EU MDR)

Ref S000393Model FASTA FCM 150, FASTA FCM 300, FASTA FCM-D 75-D, FASTA FCH 150, FASTA FCH 300, FASTA FCH-D 75-D

by GeneMind Biosciences Co., Ltd.

Identity

Trade Name
GeneMind EUDAMED
Device Name
Universal Reaction Kit for Sequencing(Reversible Terminator Sequencing) EUDAMED
Model / Reference
FASTA FCM 150, FASTA FCM 300, FASTA FCM-D 75-D, FASTA FCH 150, FASTA FCH 300, FASTA FCH-D 75-D EUDAMED
S000393 EUDAMED

Identifiers

Primary DI / UDI-DI
06974968583629 EUDAMED
Basic UDI-DI
697496858FASTASeq-Kit2W EUDAMED
Direct Marketing DI
06974968583629 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 ceeabe7e-f260-440d-a62c-6f8e5ea64ae7 61 fields · synced Jun 19, 2026