Shear Wave Quantificational Ultrasound Diagnostic System

GUDID 06971679945005

Wuxi Hisky Medical Technologies Co.,Ltd.

Hepatic ultrasound elastography system

• Primary Device ID: 06971679945005
• NIH Device Record Key: 814c2a4e-e56b-45f9-a974-a408a901522e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Shear Wave Quantificational Ultrasound Diagnostic System
• Version Model Number: FT9000
• Company DUNS: 544348534
• Company Name: Wuxi Hisky Medical Technologies Co.,Ltd.
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +8651085387702
• Email: service@hiskymedical.com

Operating and Storage Conditions

• Storage Environment Temperature: Between -5 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971679945005 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K173595

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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2020-04-08
• Device Publish Date: 2020-03-31

On-Brand Devices [Shear Wave Quantificational Ultrasound Diagnostic System]

• 06971679945005: FT9000
• 06971679949072: Mini800
• 06971679949065: FT100