Home GUDID 15060808320023 MotionSense Adhesive Refill Kit
Primary DI 15060808320023
Brand MotionSense Adhesive Refill Kit
Company ENMOVI LTD
Model MotionSense 2.0
Catalog number 007-00037-US
Published 2021-08-13
Public version status New
Distribution status In Commercial Distribution
MRI safety Labeling does not contain MRI Safety Information
Rx true
OTC false
Sterile false
Single use true Product Codes# Code, Name table Code Name KQX Goniometer, Ac-Powered
Product Code Classifications# Code, Device, Specialty table Code Device Specialty Class KQX Goniometer, Ac-Powered Orthopedic 1
Identifiers And Packaging# Identifier, Type, Agency table Identifier Type Agency Package quantity Status 15060808320023 Primary GS1 0
Alternate GTIN / UPC / EAN Codes Source identifier, GTIN-14 normalized table Source identifier GTIN-14 normalized 15060808320023 15060808320023
GMDN Terms# Term, Definition table Term Definition Electronic goniometer/kinesiology sensor A small electronic device designed to be fastened to a body part (e.g., a patient worn goniometer-, accelerometer-, or gyroscope-sensor), or hand-held by a clinician (e.g., goniometer), to evaluate a patient’s range of motion/movement of individual joints/limbs/spine; it is used in a clinical setting typically before/after a medical/surgical intervention, or to assess degree of physical fitness. Acquired data may be transferred to a computing device/software for recording/display and analysis.
Storage And Handling# Type, Low, High table Type Low High Condition Storage Environment Humidity 15 Percent (%) Relative Humidity 75 Percent (%) Relative Humidity Storage Environment Temperature 0 Degrees Celsius 25 Degrees Celsius
Regulatory Flags# DUNS number 225424353 Device count 1 DM exempt false Premarket exempt true HCT/P false Kit false Combination product false Lot or batch true Serial number false Manufacturing date on label true Expiration date on label true Donation ID number false Contains natural rubber latex false No natural rubber latex false Sterilization required before use false Other Devices From This Company# Primary DI, Brand, Model table Primary DI Brand Model Catalog Published 55060808320151 MotionSense Application Version 1.4 SW-1.4-MSAPP SW-1.4-MSAPP 2023-01-27 55060808320168 MotionSense Application Version 1.5 SW-1.5-MSAPP SW-1.5-MSAPP 2023-01-27 55060808320120 OrthoLogIQ PT Version 1.0 SW-1.0-OIQPT SW-1.0-OIQPT 2023-01-27 15060808320092 MotionSense Digital Goniometer 007-00066-US 007-00066-US 2022-07-15 15060808320108 MotionSense Adhesive Refill Kit 007-00067-US 007-00067-US 2022-07-15 15060808320115 MotionSense Knee Alignment Block 007-00068-US 007-00068-US 2022-07-15 55060808320076 MotionSense Application Version 1.3 SW-1.3-MSAPP SW-1.3-MSAPP 2022-07-15 15060808320030 MotionSense Knee Alignment Block MotionSense 2.0 007-00038-US 2021-08-13 55060808320007 MotionSense Digital Goniometer MotionSense 2.0 007-00036-US 2021-08-13
Other Devices Sharing Product Codes# 
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