SONIALVISION G4

GUDID 04540217041046

SHIMADZU CORPORATION

Stationary general-purpose fluoroscopic x-ray system, digital

• Primary Device ID: 04540217041046
• NIH Device Record Key: 8ce443f1-060b-4314-a544-ad254409cd29
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SONIALVISION G4
• Version Model Number: 566-10000-43
• 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	04540217041046 [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: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-05-28
• Device Publish Date: 2019-08-14

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
• 04540217041060: 566-10000-47
• 04540217041053: 566-10000-46
• 04540217041046: 566-10000-43
• 04540217041039: 566-10000-42
• 04540217041022: 566-10000-41
• 04540217040896: 503-78000-53
• 04540217040889: 503-78000-52
• 04540217040872: 503-78000-51