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Guidewire Ø 1.6

EUDAMED

Class I (EU MDR)

Ref STAIGW016

by BRM Extremities S.r.l.

Identity

Trade Name
Guidewire Ø 1.6 EUDAMED
Device Name
Strumenti chirurgici riutilizzabili accessori alle Viti per Osteosintesi EUDAMED
Model / Reference
STAIGW016 EUDAMED

Identifiers

Primary DI / UDI-DI
08053782780396 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

Guidewire Ø 1.6 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 0cfcab58-e4de-4052-9fd3-b7553ed0e1ec 61 fields · synced Jun 18, 2026