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STANDARD™ i2000

EUDAMED

Class A (EU MDR)

Ref 16IA200Model i2000

by SD Biosensor Inc.

Identity

Trade Name
STANDARD™ i2000 EUDAMED
Device Name
STANDARD™ i2000 EUDAMED
Model / Reference
i2000 EUDAMED
16IA200 EUDAMED

Identifiers

Primary DI / UDI-DI
08800111720260 EUDAMED
Basic UDI-DI
88001117IPAA01IA02V8 EUDAMED
Direct Marketing DI
08800111722585 EUDAMED
EMDN Code
W0201020102 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - MODERATE ROUTINE (Throughput > 100 and <= 250 test/h) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Italy 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

STANDARD™ i2000 by SD Biosensor Inc. — 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

Manufacturer
SD Biosensor Inc.
EUDAMED SRN
KR-MF-000009168
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 8da2d66b-2350-4b79-9e9a-26434205ebfb 61 fields · synced Jul 10, 2026