G-22

GUDID 04560141950795

KONICA MINOLTA, INC.

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• Primary Device ID: 04560141950795
• NIH Device Record Key: b0f27c3b-4143-4c92-bda0-9e7e05759b3a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: G-22
• Version Model Number: AE83
• 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: 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	04560141950795 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K223267

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-06-22
• Device Publish Date: 2023-06-14

Devices Manufactured by KONICA MINOLTA, INC.

• 04560141950399 - ImagePilot: 2023-07-27
• 04560141950771 - G-59: 2023-06-22
• 04560141950788 - G-60: 2023-06-22
• 04560141950795 - G-22: 2023-06-22
• 04560141950795 - G-22: 2023-06-22
• 04560141950849 - KONICAMINOLTA DI-X1: 2023-05-12
• 04560141949287 - P-65: 2022-11-25
• 04560141949294 - P-75: 2022-11-25
• 04560141950276 - P-95: 2022-11-21