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MART-1 - MART-1

EUDAMED

Class C (EU MDR)

Ref A00115-C

by ScyTek Laboratories Inc.

Identity

Trade Name
MART-1; Clone M2-7C10 (Concentrate) 1 mL EUDAMED
Device Name
Primary Antisera for Immunohistology EUDAMED
Model / Reference
A00115-C EUDAMED

Identifiers

Primary DI / UDI-DI
00810108711537 EUDAMED
Basic UDI-DI
081010871W01030709FJ EUDAMED
Direct Marketing DI
00810108711537 EUDAMED
EMDN Code
W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
Models / Variants
MART-1 EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Netherlands 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

MART-1 - MART-1 by ScyTek Laboratories Inc. — Class C — IVDR — listed in EUDAMED — 2 models — 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
US-MF-000023816
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 2d52538d-9d2b-48d1-946e-743713ec6d32 61 fields · synced Jun 18, 2026