Medistim MiraQ Cardiac System MQC04122

GUDID 07070554102492

Medistim ASA

Invasive vascular ultrasound system

• Primary Device ID: 07070554102492
• NIH Device Record Key: 19f16676-58ce-47aa-a41b-9bc050901da4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Medistim MiraQ Cardiac System
• Version Model Number: MQC04122
• Catalog Number: MQC04122
• Company DUNS: 519521751
• Company Name: Medistim ASA
• 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: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	07070554102492 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102595

FDA Product Code

• IYN: System, Imaging, Pulsed Doppler, 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: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2017-07-03

On-Brand Devices [Medistim MiraQ Cardiac System]

• 07070554103307: MQC14022
• 07070554103277: MQC14012
• 07070554102492: MQC04122
• 07070554101501: MQC14002
• 07070554101495: MQC14001
• 07070554101488: MQC12001
• 07070554101327: MQC04102
• 07070554101303: MQC04001
• 07070554101273: MQC02001