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Viper

EUDAMED

Class A (EU MDR)

Ref 441360

by Becton, Dickinson and Company

Identity

Trade Name
VIPER EUDAMED
Device Name
BD Specimen Tubes and Caps for use on the BD Viper™ System EUDAMED
Model / Reference
441360 EUDAMED

Identifiers

Primary DI / UDI-DI
30382904413607 EUDAMED
Basic UDI-DI
038290IEHRMMUH8T EUDAMED
Unit of Use DI
00382904413606 EUDAMED
EMDN Code
W02050185 NUCLEIC ACID TESTING INSTRUMENTS EXCEPT MICRO-ARRAYS - CONSUMABLES EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

No

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

Viper by Becton, Dickinson and Company — 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-000018910
Authorised Representative
Becton Dickinson Ireland Limited IE-AR-000007610

Sources (1)

  • EUDAMED ec3c1211-c29b-4492-852d-7123d79d4787 61 fields · synced Jun 9, 2026