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Optyfill

EUDAMED

Class IIa (EU MDR)

Ref OPF1110C-01EM

by Biopsybell Srl

Identity

Trade Name
OPTYFILL EUDAMED
Device Name
SUBCHONDRAL BONE MARROW LESIONS (BML) SYSTEMS EUDAMED
Model / Reference
OPF1110C-01EM EUDAMED

Identifiers

Primary DI / UDI-DI
08033860030902 EUDAMED
Basic UDI-DI
8033860SUBFT01C6H EUDAMED
EMDN Code
P099002 ORTHOPAEDIC CEMENT PREPARATION AND APPLICATION DEVICES 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

Optyfill 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 01f817e6-ab01-4b4d-82dd-17efbe872833 61 fields · synced Jun 18, 2026