AeroDR P-11

GUDID 04560141933613

KONICA MINOLTA, INC.

Indirect flat panel x-ray detector

• Primary Device ID: 04560141933613
• NIH Device Record Key: c082b97b-0656-41f7-9efb-7109833afc0f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AeroDR P-11
• Version Model Number: A7WE
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	04560141933613 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102349

FDA Product Code

• MQB: Solid State X-Ray Imager (Flat Panel/Digital Imager)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-05-07
• Device Publish Date: 2016-09-19

On-Brand Devices [AeroDR P-11]

• 04560141934719: A5DP
• 04560141933613: A7WE