SonoSite NanoMaxx P11111

GUDID 00841517101329

FUJIFILM SONOSITE, INC.

General-purpose ultrasound imaging system

• Primary Device ID: 00841517101329
• NIH Device Record Key: da80df24-73ee-417b-93a7-b83b07c30582
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: SonoSite NanoMaxx
• Version Model Number: P11111-46
• Catalog Number: P11111
• 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: xyz@xyz.com

Operating and Storage Conditions

• Handling Environment Atmospheric Pressure: Between 50 KiloPascal and 106 KiloPascal

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841517101329 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K102390

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: 2016-09-21

On-Brand Devices [SonoSite NanoMaxx]

• 00841517101336: P11111-46R
• 00841517101329: P11111-46
• 00841517100919: P11111-60R
• 00841517100902: P11111-60