AeroDR 0170CS

GUDID 04560141946262

KONICA MINOLTA, INC.

X-ray system tube support, ceiling mount

• Primary Device ID: 04560141946262
• NIH Device Record Key: 7a11194c-9341-4beb-8edd-eb9b32abde36
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AeroDR 0170CS
• Version Model Number: AACW
• Company DUNS: 692076161
• Company Name: KONICA MINOLTA, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	04560141946262 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121109

FDA Product Code

• KPR: System, X-Ray, Stationary

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: 2018-08-27
• Device Publish Date: 2018-07-26

Devices Manufactured by KONICA MINOLTA, INC.

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• 04560141950771 - G-59: 2023-06-22