Conserus Enterprise Viewer Mobile

GUDID 80010939130019

MCKESSON TECHNOLOGIES INC.

Radiology picture archiving and communication system application software

• Primary Device ID: 80010939130019
• NIH Device Record Key: 263bb24f-87f7-4452-b8f5-cdd7febe9a33
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Conserus Enterprise Viewer Mobile
• Version Model Number: 1.1
• 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: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	80010939130019 [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: 3
• Public Version Date: 2018-09-24
• Device Publish Date: 2016-08-26

Devices Manufactured by MCKESSON TECHNOLOGIES INC.

• 80010939020013 - McKesson Radiology: 2018-09-24
• 80010939020020 - McKesson Radiology: 2018-09-24
• 80010939020037 - McKesson Radiology: 2018-09-24
• 80010939020044 - McKesson Radiology: 2018-09-24
• 80010939120010 - Conserus Enterprise Viewer: 2018-09-24
• 80010939120027 - Conserus Enterprise Viewer: 2018-09-24
• 80010939130019 - Conserus Enterprise Viewer Mobile: 2018-09-24
• 80010939130019 - Conserus Enterprise Viewer Mobile: 2018-09-24
• 80010939040028 - McKesson Cardiology ECG Management: 2018-07-06