Cerner SkyVue®

GUDID 00853023006074

CERNER CORPORATION

Diagnostic x-ray digital imaging system workstation application software

• Primary Device ID: 00853023006074
• NIH Device Record Key: df19da8d-2ecb-4894-9a5e-441d3116ef9a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cerner SkyVue®
• Version Model Number: SkyVue4
• Company DUNS: 042410688
• Company Name: CERNER CORPORATION
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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	00853023006074 [Primary]

FDA Product Code

• LLZ: System, Image Processing, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2017-07-31

On-Brand Devices [Cerner SkyVue®]

• 00853023006074: SkyVue4
• 00853023006036: SkyVue2014