Cerner Motion Health

GUDID 00853023006180

CERNER CORPORATION

Biomechanical function analysis/rehabilitation software

• Primary Device ID: 00853023006180
• NIH Device Record Key: 2148aa6f-d49a-4587-a278-dd9df7953c56
• Commercial Distribution Discontinuation: 2018-04-24
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Cerner Motion Health
• Version Model Number: MotionHealth2016.22
• Company DUNS: 042410688
• Company Name: CERNER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00853023006180 [Primary]

FDA Product Code

• ISD: Exerciser, Measuring

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-06-26
• Device Publish Date: 2017-07-27

Devices Manufactured by CERNER CORPORATION

• 00850017753112 - FetaLink+: 2024-06-03
• 00850017753037 - Cerner Patient Observer: 2020-12-22
• 00853023006241 - Cerner Patient Observer: 2020-02-10
• 00853023006197 - Cerner Patient Observer: 2019-10-08
• 00853023006203 - Cerner Patient Observer: 2019-10-08
• 00853023006234 - Cerner Patient Observer: 2019-10-08
• 00853023006111 - Cerner CareAware Event Management: 2019-07-12
• 00853023006135 - Cerner CareAware Event Management: 2019-07-12