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QuadriTest CD3 FITC/CD8 PE/CD45 PerCP/CD4 APC Kit

EUDAMED

Class C (EU MDR)

Ref 8930008CEModel 50T,100T

by Agilent Biosciences (Hangzhou) Co., Ltd.

Identity

Device Name
QuadriTest CD3 FITC/CD8 PE/CD45 PerCP/CD4 APC Kit EUDAMED
Model / Reference
50T,100T EUDAMED
8930008CE EUDAMED

Identifiers

Primary DI / UDI-DI
06974501891020 EUDAMED
Basic UDI-DI
69745018900C002301W5 EUDAMED
EMDN Code
W0103080101 ANTIBODIES FOR B AND T-CELL SUBTYPING EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany 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

QuadriTest CD3 FITC/CD8 PE/CD45 PerCP/CD4 APC Kit by Agilent Biosciences (Hangzhou) Co., Ltd. — Class C — IVDR — listed in EUDAMED

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

EUDAMED SRN
CN-MF-000013066
Authorised Representative
Agilent Technologies Denmark ApS DK-AR-000001443

Sources (1)

  • EUDAMED 00753caa-8428-465a-80e9-43a7472de9ef 61 fields · synced Jun 18, 2026