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STANDARD™ i pre-Trigger

EUDAMED

Class A (EU MDR)

Ref 16PTR10Model i-PTR-01

by SD Biosensor Inc.

Identity

Trade Name
STANDARD™ i pre-Trigger EUDAMED
Device Name
STANDARD™ i pre-Trigger EUDAMED
Model / Reference
i-PTR-01 EUDAMED
16PTR10 EUDAMED

Identifiers

Primary DI / UDI-DI
08800111722691 EUDAMED
Basic UDI-DI
88001117IPAA05IA01WJ EUDAMED
Direct Marketing DI
08800111724381 EUDAMED
EMDN Code
W0201020185 AUTOMATED IMMUNOCHEMISTRY ANALYSERS - CONSUMABLES 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

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

No

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

STANDARD™ i pre-Trigger 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 c6224c56-501f-441d-9a82-310eb60516d0 61 fields · synced Jul 12, 2026