Ultrasound System SONIMAGE HS1

GUDID 04560141945470

KONICA MINOLTA, INC.

General-purpose ultrasound imaging system

• Primary Device ID: 04560141945470
• NIH Device Record Key: 65e76762-0176-4645-b910-771edabb19d5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Ultrasound System SONIMAGE HS1
• Version Model Number: A9RR
• 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	04560141945470 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162065

FDA Product Code

• IYO: System, Imaging, Pulsed Echo, Ultrasonic

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-11-09

On-Brand Devices [Ultrasound System SONIMAGE HS1]

• 04560141947436: AC7H
• 04560141947429: AC7J
• 04560141947412: AC7G
• 04560141946385: AAEU
• 04560141945470: A9RR
• 04560141945463: A9RP
• 04560141944534: A8WA
• 04560141941588: A8AR
• 04560141940031: A7AP