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NESCAUTO Cp Auto AA01

EUDAMED

Class B (EU MDR)

Ref 912682

by Alfresa Pharma Corporation

Identity

Trade Name
NESCAUTO Cp Auto AA01 EUDAMED
Device Name
NESCAUTO Cp Auto AA01 EUDAMED
Model / Reference
912682 EUDAMED

Identifiers

Primary DI / UDI-DI
04987274126826 EUDAMED
Basic UDI-DI
4987274W0102019009CPR02ZR EUDAMED
EMDN Code
W0102019009 CALPROTECTIN EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

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

NESCAUTO Cp Auto AA01 by Alfresa Pharma Corporation — 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

EUDAMED SRN
JP-MF-000008778
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 38fddc38-ed9b-4caf-9def-a71dc2635535 61 fields · synced Jul 23, 2026