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FlashDetect

EUDAMED

Class A (EU MDR)

Ref 08020003Model FM-1

by Coyote Bioscience Co., Ltd.

Identity

Trade Name
FlashDetect EUDAMED
Device Name
FlashDetect Mixer EUDAMED
Model / Reference
FM-1 EUDAMED
08020003 EUDAMED

Identifiers

Primary DI / UDI-DI
06977739174101 EUDAMED
Basic UDI-DI
697773917080200033E EUDAMED
Direct Marketing DI
06977739174101 EUDAMED
EMDN Code
W02060199 ROBOTIC SAMPLE PROCESSING SYSTEMS - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Sweden EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

Yes

EUDAMED

New Device

No

EUDAMED

FlashDetect by Coyote Bioscience 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-000024155
Authorised Representative
QbD RepS BV BE-AR-000000040

Sources (1)

  • EUDAMED 1189fe88-a5c7-42fc-b9a5-30439565233d 61 fields · synced Jun 17, 2026