← Back to catalogue

CD56 - CD56

EUDAMED

Class C (EU MDR)

Ref A00121-0007

by ScyTek Laboratories Inc.

Identity

Trade Name
CD56; Clone 123C3 (Ready-To-Use) 7 mL EUDAMED
Device Name
Primary Antisera for Immunohistology EUDAMED
Model / Reference
A00121-0007 EUDAMED

Identifiers

Primary DI / UDI-DI
00810108711698 EUDAMED
Basic UDI-DI
081010871W01030709FJ EUDAMED
Direct Marketing DI
00810108711698 EUDAMED
EMDN Code
W01030709 PRIMARY ANTISERA FOR IMMUNOHISTOLOGY EUDAMED
Models / Variants
CD56 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

CD56 - CD56 by ScyTek Laboratories Inc. — Class C — IVDR — listed in EUDAMED — 2 models — regulatory data on deviCERTS

Manufacturer's product page: Hairy Cell Leukemia; Clone DBA.44 (Ready-To-Use) SKU: A00015 Antibodies, Monoclonal

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

EUDAMED SRN
US-MF-000023816
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (1)

  • EUDAMED 030579b1-69e2-491f-9b64-320919d97483 61 fields · synced Jun 19, 2026