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Somacore Verify S

EUDAMED

Class IIa (EU MDR)

Ref 900506-US

by Biopsybell Srl

Identity

Trade Name
SOMACORE VERIFY S EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
Model / Reference
900506-US EUDAMED

Identifiers

Primary DI / UDI-DI
08033860023447 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
EMDN Code
A0102010102 SHEARING BIOPSY GUNS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Germany EUDAMED

Clinical & Handling

Sterile

Yes

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Somacore Verify S by Biopsybell Srl — Class IIa — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (1)

  • EUDAMED b91c7583-0ad1-4a69-a0a0-c1d341612a17 61 fields · synced Jun 18, 2026