ENMOVI LTD

Address:Unit 1l, Inovo Building,Glasgow,GB

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Filters

Device Class

Class-1 (A medical device with low to moderate risk that requires general controls) Class-2 (A medical device with a moderate to high risk that requires special controls) Class-3 (A medical device with high risk that requires premarket approval) Class-U (Unclassified)

Product Code

Goniometer, Ac-Powered (KQX) (7)

Premarket Exempt

Yes

Clear

MotionSense Adhesive Refill Kit - 15060808320023 Catalog Number : 007-00037-US

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

MotionSense Knee Alignment Block - 15060808320030 Catalog Number : 007-00038-US

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

MotionSense Digital Goniometer - 15060808320092 Catalog Number : 007-00066-US

Device Description : MotionSense Digital Goniometer

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

MotionSense Adhesive Refill Kit - 15060808320108 Catalog Number : 007-00067-US

Device Description : MotionSense Adhesive Refill Kit

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

MotionSense Knee Alignment Block - 15060808320115 Catalog Number : 007-00068-US

Device Description : MotionSense Knee Alignment Block

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

MotionSense Digital Goniometer - 55060808320007 Catalog Number : 007-00036-US

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

MotionSense Application Version 1.3 - 55060808320076 Catalog Number : SW-1.3-MSAPP

Device Description : MotionSense Application Version 1.3

Device Class : 1

Duns Number: 225424353

Premarket Exempt : Yes

Product Code : KQX

Prescription Use : Yes

Device Count : 1

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