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WISE (wireless inertial sensor equipment)

FDA UDI

Class II (US FDA UDI)

by Ncs Lab Srl

Identity

Trade Name
WISE (wireless inertial sensor equipment) FDA UDI
Generic Name
Electronic goniometer/kinesiology sensor FDA UDI
Device Name
The WISE is a magnetic and inertial unit including 3D accelerometers, gyroscopes and magnetometers. FDA UDI
Model / Reference
WISE01 FDA UDI
Description
The WISE is a magnetic and inertial unit including 3D accelerometers, gyroscopes and magnetometers. FDA UDI

Identifiers

Primary DI / UDI-DI
08051122041008 FDA UDI
FDA Product Code
ISD FDA UDI
GMDN Term
Electronic goniometer/kinesiology sensor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.5360 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

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

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Electronic goniometer/kinesiology sensor

WISE (wireless inertial sensor equipment) by Ncs Lab Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electronic goniometer/kinesiology sensor.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ncs Lab Srl

Sources (1)

  • FDA UDI 2fca9b0d-2c5f-4098-95c2-5859b5a792b8 34 fields · synced May 31, 2026