McKesson Radiology

GUDID 80010939020013

MCKESSON TECHNOLOGIES INC.

Radiology picture archiving and communication system application software

• Primary Device ID: 80010939020013
• NIH Device Record Key: 0f5181cc-b954-4ec0-805f-39970652d1e7
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: McKesson Radiology
• Version Model Number: 12.2.1
• Company DUNS: 962049362
• Company Name: MCKESSON TECHNOLOGIES INC.
• 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: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	80010939020013 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140909

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: 4
• Public Version Date: 2018-09-24
• Device Publish Date: 2016-09-23

On-Brand Devices [McKesson Radiology]

• 80010939020044: 12.2.3
• 80010939020037: 12.3
• 80010939020020: 12.2.2
• 80010939020013: 12.2.1