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Vitek® 2 Ast-Xn40

EUDAMED

Class B (EU MDR)

Ref 543660

by bioMérieux, Inc.

Identity

Trade Name
VITEK® 2 AST-XN40 EUDAMED
Device Name
VITEK® 2 AST-XN40 EUDAMED
Model / Reference
543660 EUDAMED

Identifiers

Primary DI / UDI-DI
03573026642037 EUDAMED
Basic UDI-DI
357302BUDI002261TN EUDAMED
EMDN Code
W0104080107 GRAM NEGATIVE SUSCEPTIBILITY TESTING - AUTOMATED EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

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

Category: General-microorganism antimicrobial susceptibility culture medium IVD

Vitek® 2 Ast-Xn40 by Biomérieux — Class B — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General-microorganism antimicrobial susceptibility culture medium IVD.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
bioMérieux, Inc.
EUDAMED SRN
US-MF-000011802
Authorised Representative
bioMérieux SA FR-AR-000004435

Sources (1)

  • EUDAMED b2f1b46a-9933-4e67-8617-531fe3900296 61 fields · synced Jul 12, 2026