Cadi CADI

GUDID 10667147001559

Cadi Software

Synca Marketing Inc

Radiology information system application software

• Primary Device ID: 10667147001559
• NIH Device Record Key: f43ac327-9d8d-47cb-bedc-b96a3c9fa1d0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Cadi
• Version Model Number: V8
• Catalog Number: CADI
• Company DUNS: 247111768
• Company Name: Synca Marketing 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: false
• Serial Number: false
• Manufacturing Date: false
• 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	10667147001559 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K062237

FDA Product Code

• LLZ: System, Image Processing, Radiological

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: 2025-07-08
• Device Publish Date: 2021-07-15

On-Brand Devices [Cadi]

• 00066714700155: Cadi Software
• 10667147001559: Cadi Software