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Substrat/Substrate LINE

EUDAMED

Class A (EU MDR)

Ref WE200.02

by Gold Standard Diagnostics Frankfurt GmbH

Identity

Trade Name
Substrat/Substrate LINE EUDAMED
Device Name
Substrat/Substrate LINE EUDAMED
Model / Reference
WE200.02 EUDAMED

Identifiers

Primary DI / UDI-DI
+ENTIWE2000203 EUDAMED
Basic UDI-DI
++ENTIWE20002V036A EUDAMED
Direct Marketing DI
+ENTIWE2000203 EUDAMED
EMDN Code
W0105900201 BUFFERS (UNASSIGNABLE ), SUPPLEM. REAGENTS, ETC EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Germany 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

Substrat/Substrate LINE by Gold Standard Diagnostics Frankfurt GmbH — 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
DE-MF-000025020

Sources (1)

  • EUDAMED 3e7581e9-0778-4e69-b4d0-2fc361a6aca4 61 fields · synced Jun 18, 2026