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Universal Sequencing Reaction Kit T7 SM FCL SE35

EUDAMED

Class A (EU MDR)

Ref 1000022498

by Wuhan MGI Tech Co., Ltd.

Identity

Trade Name
Universal Sequencing Reaction Kit T7 SM FCL SE35 EUDAMED
Device Name
Universal Sequencing Reaction Kit EUDAMED
Model / Reference
1000022498 EUDAMED

Identifiers

Primary DI / UDI-DI
06974318130268 EUDAMED
Basic UDI-DI
697431813S-KitMW EUDAMED
Direct Marketing DI
06974318130268 EUDAMED
EMDN Code
W010699 GENETIC TESTS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Latvia 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

Universal Sequencing Reaction Kit T7 SM FCL SE35 by Wuhan MGI Tech 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-000018732
Authorised Representative
Shanghai International Holding Corp. GmbH(Europe) DE-AR-000000001

Sources (1)

  • EUDAMED 93f2ed13-4587-44d4-9ce9-d1e4e6eb5806 61 fields · synced Jun 20, 2026