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Navigation Sensor

EUDAMEDFDA UDI

Class IIa (EU MDR)

Ref A 01 1000Model Cube 4D Navigation System

by Fiagon GmbH

Identity

Trade Name
Navigation Sensor EUDAMEDFDA UDI
Generic Name
Multi-purpose stereotactic surgery system FDA UDI
Device Name
Field generating device of electromagnetic navigation system Cube4D (image guided surgery). The device is component of the Cube4D Navigation system. FDA UDI
Model / Reference
Cube 4D Navigation System EUDAMED
A 01 1000 EUDAMED
A011000 FDA UDI
Description
Field generating device of electromagnetic navigation system Cube4D (image guided surgery). The device is component of the Cube4D Navigation system. FDA UDI

Identifiers

Catalog Number
A011000 FDA UDI
Primary DI / UDI-DI
04260759930249 EUDAMEDFDA UDI
Basic UDI-DI
426075993E1006C EUDAMED
Direct Marketing DI
04260759930249 EUDAMED
FDA Product Code
PGW FDA UDI
EMDN Code
Z12011401 SURGICAL NAVIGATION SYSTEM EUDAMED
GMDN Term
Multi-purpose stereotactic surgery system FDA UDI

Classification

Device Class
Class IIa EUDAMED
Class II FDA UDI
Regulation Number
882.4560 FDA UDI
Market of Registration
Germany EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Navigation Sensor by Fiagon GmbH — Class IIa — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Fiagon GmbH
EUDAMED SRN
DE-MF-000010763

Sources (2)

  • EUDAMED c65e8a33-b430-4174-b4da-08624a534419 61 fields · synced May 30, 2026
  • FDA UDI db0c472f-1e05-4564-9b64-0b4b5c2c6edb 35 fields · synced May 30, 2026