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Streptavidin/HRP

EUDAMED

Class A (EU MDR)

Ref P0397Model P039701-2

by Agilent Technologies Singapore (International) Pte Ltd

Identity

Trade Name
Streptavidin/HRP EUDAMED
Device Name
Streptavidin/HRP EUDAMED
Model / Reference
P039701-2 EUDAMED
P0397 EUDAMED

Identifiers

Primary DI / UDI-DI
05700572007609 EUDAMED
Basic UDI-DI
570057P3007P3010A055101NR EUDAMED
EMDN Code
W01029003 BUFFERS (UNASSIGNABLE), SUPPLEM. REAGENTS, ETC (IC) 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

Streptavidin/HRP 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 638a1ae1-05e6-4f82-8eb4-8bb8d809cf62 61 fields · synced Jun 19, 2026