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3F-Fit Fabricando Faber d.o.o. Beograd-Čukarica

Serbia·RS-MF-000020496

Last updated September 17, 2026

What 3F-Fit Fabricando Faber d.o.o. Beograd-Čukarica makes

3F-Fit Fabricando Faber produces wearable and footwear devices designed for neurological and motor function monitoring, including insoles, garments, and shoes integrated into the NeuroSkin System. The Motimove-8 appears to be a mobility or rehabilitation device, while the HephaBike is likely a cycling-related assistive or monitoring system.

The company’s portfolio includes Class I and Class IIa medical devices, all registered in the EU’s eudamed database. The devices are manufactured in Serbia.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does 3F-Fit Fabricando Faber manufacture?

3F-Fit Fabricando Faber manufactures wearable and footwear devices focused on neurological and motor function monitoring. Their portfolio includes insoles, garments, shoes, and systems like the NeuroSkin System, which integrates multiple components for monitoring purposes. They also produce the Motimove-8, likely a mobility or rehabilitation device, and the HephaBike, which appears to be a cycling-related assistive or monitoring system.

Where is 3F-Fit Fabricando Faber based, and where are their devices manufactured?

3F-Fit Fabricando Faber is based in Beograd-Čukarica, Serbia. All their listed devices are manufactured in Serbia, as indicated by their company details.

Which regulatory registries list 3F-Fit Fabricando Faber’s devices?

3F-Fit Fabricando Faber’s devices are listed in the EU’s eudamed database, which is the official registry for medical devices under EU regulations. This ensures transparency and traceability of their products within the European market.

How are 3F-Fit Fabricando Faber’s devices classified under EU regulations?

3F-Fit Fabricando Faber’s devices fall into Class I and Class IIa classifications under EU medical device regulations. Class I devices are generally low-risk, while Class IIa devices pose a slightly higher risk and require additional conformity assessments to ensure safety and performance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Serbia
Address
41, Veljka Petrovića, Belgrade, Serbia
Website
www.3-x-f.com

This website did not respond when we last checked — the domain may no longer be active. Last checked 2026-09-18.

LinkedIn
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Facebook
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Phone
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PRRC Contact
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EUDAMED SRN
RS-MF-000020496
FDA FEI Number
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DUNS Number
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Catalogue (7)

DeviceModel / ReferenceRegistriesClassStatus
NeuroSkin Shoes NSS
EUDAMED
Class IActive
Neuroskin Garment NSKG
EUDAMED
Class IActive
NeuroSkin System NSKSYS
EUDAMED
Class IIaActive
Neuroskin Insoles NSI
EUDAMED
Class IActive
HephaBike HPBKSYS
EUDAMED
Class IIaActive
NeuroSkin Pants NSP
EUDAMED
Class IActive
Motimove-8 MM8
EUDAMED
Class IIaActive

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