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Mycoplasma

EUDAMED

Class A (EU MDR)

Ref 42507

by bioMérieux SA

Identity

Trade Name
Mycoplasma EUDAMED
Device Name
Mycoplasma EUDAMED
Model / Reference
42507 EUDAMED

Identifiers

Primary DI / UDI-DI
03573026073817 EUDAMED
Basic UDI-DI
357302BUDI000106ST EUDAMED
Unit of Use DI
03573026588663 EUDAMED
EMDN Code
W0104080207 MYCOPLASMA / UREAPLASMA - (INCL. COMBINED ID-AST) EUDAMED

Classification

Device Class
Class A 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

Mycoplasma by Biomerieux Sa — 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

Manufacturer
bioMérieux SA
EUDAMED SRN
FR-MF-000004436

Sources (1)

  • EUDAMED cc26ef4d-9059-4552-b853-a6384912110e 61 fields · synced Aug 4, 2026