CS-7

GUDID 04560141951426

KONICA MINOLTA, INC.

Diagnostic x-ray digital imaging system workstation application software

• Primary Device ID: 04560141951426
• NIH Device Record Key: 6541212d-0df5-4d4f-9f9b-d5c87f0d1289
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CS-7
• Version Model Number: AEVE
• Company DUNS: 692076161
• Company Name: KONICA MINOLTA, 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: true
• 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	04560141951426 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K241319

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: 2025-04-22
• Device Publish Date: 2025-04-14

On-Brand Devices [CS-7]

• 04560141945166: A4C1
• 04560141951419: AEVD
• 04560141951426: AEVE