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Dako REAL Antibody Diluent

EUDAMED

Class A (EU MDR)

Ref S2022Model S202230-2

by Agilent Technologies Singapore (International) Pte Ltd

Identity

Trade Name
Dako REAL Antibody Diluent EUDAMED
Device Name
Dako REAL Antibody Diluent EUDAMED
Model / Reference
S202230-2 EUDAMED
S2022 EUDAMED

Identifiers

Primary DI / UDI-DI
05700572008798 EUDAMED
Basic UDI-DI
570057P3007P3010A053401NS 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

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

Dako REAL Antibody Diluent 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 5b588edb-d320-4fcb-9765-b471e258c810 61 fields · synced Jul 28, 2026