AeroDR T50

GUDID 04560141935372

KONICA MINOLTA, INC.

Basic diagnostic x-ray system table, powered

• Primary Device ID: 04560141935372
• NIH Device Record Key: fa3ae596-9074-47d4-9667-90a4ed669982
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AeroDR T50
• Version Model Number: A4UW
• 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	04560141935372 [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: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-12-15

Devices Manufactured by KONICA MINOLTA, INC.

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• 04560141950887 - P-53: 2024-12-16
• 04560141950894 - P-53: 2024-12-16
• 04560141951419 - CS-7: 2024-12-16
• 04560141951914 - KONICAMINOLTA DI-X1: 2024-10-15
• 04560141951433 - Bone Suppression Software: 2024-07-16
• 04560141950399 - ImagePilot: 2023-07-27
• 04560141950771 - G-59: 2023-06-22