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Progesterone Saliva ELISA

EUDAMED

Class B (EU MDR)

Ref RE52281

by IBL International GmbH

Identity

Trade Name
Progesterone Saliva ELISA EUDAMED
Device Name
Progesterone Saliva ELISA EUDAMED
Model / Reference
RE52281 EUDAMED

Identifiers

Primary DI / UDI-DI
04049325030268 EUDAMED
Basic UDI-DI
4049325IVR06080005BTT EUDAMED
Direct Marketing DI
04049325030268 EUDAMED
EMDN Code
W0102050106 PROGESTERONE EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

Yes

EUDAMED

Microbial Substances

No

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

Progesterone Saliva ELISA by Ibl International Gmbh — 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
DE-MF-000015709

Sources (1)

  • EUDAMED e578a698-aa3a-4766-be9f-f1837a5a1e97 61 fields · synced Jul 24, 2026