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KinetikosMovD

FDA UDI

Class II (US FDA UDI)

by Kinetikos - Driven Solutions, S.a.

Identity

Trade Name
KinetikosMovD FDA UDI
Generic Name
Biomechanical function analysis/rehabilitation software FDA UDI
Model / Reference
0,1 FDA UDI

Identifiers

Primary DI / UDI-DI
05600638781835 FDA UDI
FDA Product Code
GZM FDA UDI
GMDN Term
Biomechanical function analysis/rehabilitation software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.1020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

Yes

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Biomechanical function analysis/rehabilitation software

KinetikosMovD by Kinetikos - Driven Solutions, S.a. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Biomechanical function analysis/rehabilitation software.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Kinetikos - Driven Solutions, S.a.

Sources (1)

  • FDA UDI f59501c3-c15e-46af-aef7-0b35fa0e6b58 32 fields · synced Jun 1, 2026