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Dako Harris Hematoxylin

EUDAMED

Class A (EU MDR)

Ref CS709Model CS70930-2

by Agilent Technologies Singapore (International) Pte Ltd

Identity

Trade Name
Dako Harris Hematoxylin EUDAMED
Device Name
Dako Harris Hematoxylin EUDAMED
Model / Reference
CS70930-2 EUDAMED
CS709 EUDAMED

Identifiers

Primary DI / UDI-DI
05700572035442 EUDAMED
Basic UDI-DI
570057P3007P3010A029001NF EUDAMED
EMDN Code
W01030708 STAIN SOLUTIONS (HISTOLOGY/CYTOLOGY) EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Denmark 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

Dako Harris Hematoxylin by Agilent Technologies Singapore (International) Pte Ltd — Class A — 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
SG-MF-000014448
Authorised Representative
Agilent Technologies Denmark ApS DK-AR-000001443

Sources (1)

  • EUDAMED 8518b390-7c0e-4636-a128-170b569f9c5b 61 fields · synced Jul 22, 2026