Merge Universal Viewer

GUDID 00842000101222

MERGE HEALTHCARE SOLUTIONS INC.

Radiology picture archiving and communication system workstation

• Primary Device ID: 00842000101222
• NIH Device Record Key: ed3c89e2-7023-43c5-a1ea-811f97edae88
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Merge Universal Viewer
• Version Model Number: 9.1
• 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	00842000101222 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K250301

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: 2025-08-11
• Device Publish Date: 2025-08-01

On-Brand Devices [Merge Universal Viewer]

• 00842000101093: 8.3
• 00842000101130: 8.4
• 00842000101161: 8.5
• 00842000101222: 9.1