Vevo MD Imaging System VS-20048-50

GUDID 00841517104726

Diagnostic ultrasound system

FUJIFILM SONOSITE, INC.

General-purpose ultrasound imaging system

• Primary Device ID: 00841517104726
• NIH Device Record Key: 1f90049e-f9dc-4675-9846-e1065b1393af
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Vevo MD Imaging System
• Version Model Number: 51475-50
• Catalog Number: VS-20048-50
• Company DUNS: 014438860
• Company Name: FUJIFILM SONOSITE, 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: 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: +1(999)999-9999
• Email: xx@xx.xx

Operating and Storage Conditions

• Handling Environment Temperature: Between -35 Degrees Celsius and 50 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841517104726 [Primary]

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: 2
• Public Version Date: 2020-03-02
• Device Publish Date: 2019-04-05

On-Brand Devices [Vevo MD Imaging System]

• 00841517104726: Diagnostic ultrasound system
• 00841517103248: Diagnostic ultrasound system
• 00841517102548: Diagnostic ultrasound system
• 00841517102524: Diagnostic ultrasound system
• 00841517100766: Diagnostic ultrasound system
• 00841517100759: Diagnostic ultrasound system
• 00841517109790: Diagnostic ultrasound system
• 00841517110123: Diagnostic ultrasound system