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Temocillin 30 (w) E112038

EUDAMED

Class B (EU MDR)

Ref E112038 (W)

by BioMaxima Spółka Akcyjna

Identity

Device Name
TEMOCILLIN 30 (W) E112038 EUDAMED
Model / Reference
E112038 (W) EUDAMED

Identifiers

Primary DI / UDI-DI
05902643982680 EUDAMED
Basic UDI-DI
59026439BASTTEMSH EUDAMED
EMDN Code
W0104080502 IMPREGNATED DISKS, MULTI-DISKS & TABLETS EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Poland 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

Temocillin 30 (w) E112038 by BioMaxima Spółka Akcyjna — 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
PL-MF-000039473

Sources (1)

  • EUDAMED d1cd23ab-302f-467f-9cef-ada7b688d190 61 fields · synced Jul 8, 2026