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Pregnenolone sulfate LC-MS/MS

EUDAMED

Class B (EU MDR)

Ref YM2000

by Immundiagnostik AG

Identity

Trade Name
Pregnenolone sulfate LC-MS/MS EUDAMED
Device Name
Pregnenolone sulfate LC-MS/MS EUDAMED
Model / Reference
YM2000 EUDAMED

Identifiers

Primary DI / UDI-DI
04050598012707 EUDAMED
Basic UDI-DI
4050598DVPhysiolW8 EUDAMED
Direct Marketing DI
04050598012707 EUDAMED
EMDN Code
W0102069099 INDIVIDUAL AND SPECIFIC HORMONES - OTHER EUDAMED

Classification

Device Class
Class B EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

Yes

EUDAMED

Pregnenolone sulfate LC-MS/MS by Immundiagnostik AG — 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

Manufacturer
Immundiagnostik AG
EUDAMED SRN
DE-MF-000020905

Sources (1)

  • EUDAMED 7664d3dd-706a-4f8e-be7b-d06fd53343dc 61 fields · synced Jun 19, 2026