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K-Move

EUDAMEDFDA UDI

Class I (EU MDR)

Ref MP.08.03.FN

by KINVENT Biomecanique

Identity

Trade Name
K-Move EUDAMED
KForce Sens FDA UDI
Generic Name
Electronic goniometer/kinesiology sensor FDA UDI
Device Name
KForce Sens EUDAMED
K Move is an inertial sensor to measure the range of motion and to compare the symmetry between the injured limb’s amplitude and the healthy limb. FDA UDI
Model / Reference
MP.08.03.FN EUDAMED
K Move V3 FDA UDI
Description
K Move is an inertial sensor to measure the range of motion and to compare the symmetry between the injured limb’s amplitude and the healthy limb. FDA UDI

Identifiers

Primary DI / UDI-DI
03770011995462 EUDAMEDFDA UDI
Basic UDI-DI
B-03770011995462 EUDAMED
FDA Product Code
KQX FDA UDI
EMDN Code
V030202 GONIOMETERS EUDAMED
GMDN Term
Electronic goniometer/kinesiology sensor FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
888.1500 FDA UDI
Market of Registration
France 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

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

No

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

K-Move by Kinvent Biomecanique — Class I — MDD, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDD

United States Pending data

FDA UDI

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Manufacturer

EUDAMED SRN
FR-MF-000031884

Sources (2)

  • EUDAMED 69cfa269-da24-4b39-81df-3ff116179f63 61 fields · synced Jun 20, 2026
  • FDA UDI 9e68a6c5-c8f1-4e34-920c-5c96daadb081 35 fields · synced May 30, 2026