Aquilion Exceed LB

GUDID 04987670104121

CANON MEDICAL SYSTEMS CORPORATION

Full-body CT system

• Primary Device ID: 04987670104121
• NIH Device Record Key: 730baa02-0574-47d6-b3b1-376dfbf62c25
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Aquilion Exceed LB
• Version Model Number: TSX-202A
• Company DUNS: 690575113
• Company Name: CANON MEDICAL SYSTEMS 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: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• 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	04987670104121 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K203042

FDA Product Code

• JAK: System, X-Ray, Tomography, Computed

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: 2025-01-22
• Device Publish Date: 2025-01-14

Devices Manufactured by CANON MEDICAL SYSTEMS CORPORATION

• 04987670104121 - Aquilion Exceed LB: 2025-01-22
• 04987670104121 - Aquilion Exceed LB: 2025-01-22
• 04987670105579 - Aquilion ONE: 2025-01-17
• 04987670104541 - DIAGNOSTIC ULTRASOUND SYSTEM: 2024-07-15
• 04987670104558 - DIAGNOSTIC ULTRASOUND SYSTEM: 2024-07-15
• 04987670106095 - Aquilion Serve SP: 2024-07-12
• 04987670100925 - BIOPSY ADAPTOR: 2024-04-22
• 04987670104626 - LINEAR ARRAY TRANSDUCER: 2024-04-22
• 04987670104633 - LINEAR ARRAY TRANSDUCER: 2024-04-22