SONIALVISION G4

GUDID 04540217040957

SHIMADZU CORPORATION

Stationary general-purpose fluoroscopic x-ray system, digital

• Primary Device ID: 04540217040957
• NIH Device Record Key: ca3e6528-1322-4d79-9eff-a50e589d7784
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONIALVISION G4
• Version Model Number: 503-78000-26
• Company DUNS: 690558747
• Company Name: SHIMADZU 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: true
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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	04540217040957 [Primary]

FDA Product Code

• JAA: System, X-Ray, Fluoroscopic, Image-Intensified

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: 2018-10-29
• Device Publish Date: 2018-09-28

On-Brand Devices [SONIALVISION G4]

• 04540217040964: 503-78000-27
• 04540217040957: 503-78000-26
• 04540217040926: 503-78000-23
• 04540217064816: 503-78000-54
• 04540217064809: 503-78000-24