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Franseen

EUDAMED

Class IIa (EU MDR)

Ref FR1815EC

by Biopsybell Srl

Identity

Trade Name
FRANSEEN EUDAMED
Device Name
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
FRANSEEN EUDAMED
Model / Reference
FR1815EC EUDAMED

Identifiers

Primary DI / UDI-DI
08033860020903 EUDAMED
Basic UDI-DI
8033860BIOEFT01U5 EUDAMED
B-08033860020903 EUDAMED
EMDN Code
A01020102 ASPIRATION FINE NEEDLES AND KITS EUDAMED

Classification

Device Class
Class IIa EUDAMED
Market of Registration
Italy 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

Franseen by Biopsybell Srl — Class IIa — MDD, MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDD

European Union Active

CE/MDR

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED 06272a61-bcf8-4cc4-a304-22b0abc832b9 61 fields · synced Jul 8, 2026
  • EUDAMED 806b588b-2d48-4b1c-8918-715a6105080f 61 fields · synced May 19, 2026