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B·R·A·H·M·S Calcitonin RIA

EUDAMED

Class C (EU MDR)

Ref 529.096

by B·R·A·H·M·S GmbH

Identity

Trade Name
B·R·A·H·M·S Calcitonin RIA EUDAMED
Device Name
B·R·A·H·M·S Calcitonin RIA EUDAMED
Model / Reference
529.096 EUDAMED

Identifiers

Primary DI / UDI-DI
04260157635296 EUDAMED
Basic UDI-DI
426015763529BCalcitoRXXPU EUDAMED
EMDN Code
W0102060301 CALCITONIN EUDAMED

Classification

Device Class
Class C EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

Yes

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

B·R·A·H·M·S Calcitonin RIA by B.R.A.H.M.S GmbH — Class C — 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-000026030

Sources (1)

  • EUDAMED 93b1dabf-80bc-4628-ae21-87e527cb2568 61 fields · synced Aug 4, 2026