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Dako Antibody Diluent with Background Reducing Components

EUDAMED

Class A (EU MDR)

Ref S3022Model S302281-2

by Agilent Technologies, Inc.

Identity

Trade Name
Dako Antibody Diluent with Background Reducing Components EUDAMED
Device Name
Dako Antibody Diluent with Background Reducing Components EUDAMED
Model / Reference
S302281-2 EUDAMED
S3022 EUDAMED

Identifiers

Primary DI / UDI-DI
05700571104675 EUDAMED
Basic UDI-DI
570057P3007P3010A053701P9 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 Antibody Diluent with Background Reducing Components by Agilent Technologies, Inc. — 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
US-MF-000009385
Authorised Representative
Agilent Technologies Denmark ApS DK-AR-000001443

Sources (1)

  • EUDAMED 6b4b909b-429d-42e7-bc4b-2e65c070fce7 61 fields · synced Jun 18, 2026