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Probe – Bioplan

EUDAMED

Class I (EU MDR)

Ref SBPI10S001

by BRM Extremities S.r.l.

Identity

Trade Name
Probe – Bioplan EUDAMED
Device Name
Strumenti chirurgici riutilizzabili accessori all'impianto dei dispositivi Bioplan EUDAMED
Model / Reference
SBPI10S001 EUDAMED

Identifiers

Primary DI / UDI-DI
08057717553727 EUDAMED
Basic UDI-DI
805771755FT08C4C7 EUDAMED
EMDN Code
L091199 ORTHOPAEDIC PROSTHETICS INSTRUMENTS, REUSABLE - OTHER EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Probe – Bioplan by BRM Extremities S.r.l. — Class I — 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

EUDAMED SRN
IT-MF-000016087

Sources (1)

  • EUDAMED 567f2a39-9c97-4305-a6be-a5525b370573 61 fields · synced Jul 17, 2026