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Optymarrow

EUDAMED

Class IIa (EU MDR)

Ref OPM1110C-01

by Biopsybell Srl

Identity

Trade Name
OPTYMARROW EUDAMED
Device Name
OPTYMARROW EUDAMED
NEEDLES FOR BIOPSY OR EXPLANT EUDAMED
Model / Reference
OPM1110C-01 EUDAMED

Identifiers

Primary DI / UDI-DI
08033860032234 EUDAMED
Basic UDI-DI
B-08033860032234 EUDAMED
8033860BIOEFT01U5 EUDAMED
EMDN Code
A01020202 BONE MARROW EXPLANT 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

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

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

European Union Active

CE/MDD

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Manufacturer

Manufacturer
Biopsybell Srl
EUDAMED SRN
IT-MF-000011601

Sources (2)

  • EUDAMED d5d13fc8-0fda-48e8-b019-ffd67309d478 61 fields · synced Jul 9, 2026
  • EUDAMED c2e02d19-a90f-4021-bfef-20a04d5be132 61 fields · synced May 19, 2026