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Phoenix

EUDAMED

Class B (EU MDR)

Ref 449001

by Becton, Dickinson and Company

Identity

Trade Name
Phoenix EUDAMED
Device Name
BD Phoenix™ NMIC-417 EUDAMED
Model / Reference
449001 EUDAMED

Identifiers

Primary DI / UDI-DI
30382904490011 EUDAMED
Basic UDI-DI
038290RWNBPIFUL4 EUDAMED
Unit of Use DI
00382904490010 EUDAMED
EMDN Code
W0104080107 GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Belgium EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

Yes

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

Phoenix by Becton, Dickinson and Company — Class B — 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 a0c0ca2c-6570-4e19-8e31-8a3778457c3a 61 fields · synced Oct 10, 2026