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Parallel Guidewire

EUDAMED

Class I (EU MDR)

Ref STVIGW015

by BRM Extremities S.r.l.

Identity

Trade Name
Parallel Guidewire EUDAMED
Device Name
Strumenti chirurgici riutilizzabili accessori alle Viti per Osteosintesi EUDAMED
Model / Reference
STVIGW015 EUDAMED

Identifiers

Primary DI / UDI-DI
08053782781676 EUDAMED
Basic UDI-DI
805771755FT08C1BZ EUDAMED
EMDN Code
L0922 ORTHOPAEDIC SURGERY GUIDES, REUSABLE 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

Parallel Guidewire 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 478164c5-c0bb-4f95-8b93-a72d6ef4d0b8 61 fields · synced Jul 29, 2026