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Hybrid Reference Frame

EUDAMED

Class I (EU MDR)

Ref 9736511

by Medtronic Navigation Inc.

Identity

Device Name
Hybrid Reference Frame EUDAMED
Model / Reference
9736511 EUDAMED

Identifiers

Primary DI / UDI-DI
00763000989927 EUDAMED
Basic UDI-DI
0763000B00033838G EUDAMED
EMDN Code
Z12011480 SURGICAL NAVIGATION INSTRUMENTS - HARDWARE ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Netherlands EUDAMED

Clinical & Handling

Sterile

No

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

Category: Neurological stereotactic surgery system

Hybrid Reference Frame by Medtronic Navigation, Inc. — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Neurological stereotactic surgery system.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000023263
Authorised Representative
Medtronic B.V. NL-AR-000006050

Sources (1)

  • EUDAMED f9af3766-a9ba-4bde-91d2-a33aa317300b 61 fields · synced Jun 19, 2026