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master diagnóstica

EUDAMED

Class A (EU MDR)

Ref MAD-001815QK

by Vitro, S.a.

Identity

Trade Name
master diagnóstica EUDAMED
Device Name
Immunophosphatase AP Kit (Red) EUDAMED
Model / Reference
MAD-001815QK EUDAMED

Identifiers

Primary DI / UDI-DI
08435421232020 EUDAMED
Basic UDI-DI
8435421200460XW EUDAMED
Direct Marketing DI
08435421232020 EUDAMED
EMDN Code
W01030711 IMMUNOHISTOLOGY KITS EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Spain 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

Category: Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry

master diagnóstica by Vitro, S.a. — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Immunohistochemistry antibody detection IVD, kit, enzyme immunohistochemistry.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Vitro, S.a.
EUDAMED SRN
ES-MF-000001498

Sources (1)

  • EUDAMED d6d538ad-00a5-48f9-b518-e2ebc226bfaa 61 fields · synced Jun 17, 2026