eFilm Workstation

GUDID 00842000100850

Standalone software application

MERGE HEALTHCARE SOLUTIONS INC.

Radiology PACS software

• Primary Device ID: 00842000100850
• NIH Device Record Key: 269d5d9c-d753-48ac-84f7-e53fd0b3e7b3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: eFilm Workstation
• Version Model Number: 4.3
• Company DUNS: 065626069
• Company Name: MERGE HEALTHCARE SOLUTIONS 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: true
• 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	00842000100850 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K020995

FDA Product Code

• LLZ: System, Image Processing, Radiological

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2021-02-16
• Device Publish Date: 2021-02-08

On-Brand Devices [eFilm Workstation]

• 00842000100652: 4.2.1
• 00842000100287: Standalone software application
• 00842000100850: Standalone software application