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ComboStik 13

EUDAMED

Class B (EU MDR)

Ref 2C04Model ComboStik Series

by DFI Co., Ltd.

Identity

Trade Name
ComboStik 13 EUDAMED
Device Name
ComboStik Series EUDAMED
Model / Reference
ComboStik Series EUDAMED
2C04 EUDAMED

Identifiers

Primary DI / UDI-DI
08806141304715 EUDAMED
Basic UDI-DI
88061413US32D0JH EUDAMED
EMDN Code
W01010999 MULTIPLE PARAMETERS URINE TESTING - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany 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

No

EUDAMED

New Device

No

EUDAMED

ComboStik 13 by DFI Co., Ltd. — Class B — 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
DFI Co., Ltd.
EUDAMED SRN
KR-MF-000015786
Authorised Representative
MDSS GmbH DE-AR-000005430

Sources (1)

  • EUDAMED 9e0ca9da-983d-432d-a065-ff2c10affb5b 61 fields · synced Jun 18, 2026