P21xp/5-1 MHz

GUDID 00841517101145

Diagnostic Ultrasound Transducer

FUJIFILM SONOSITE, INC.

Extracorporeal ultrasound imaging transducer, hand-held

• Primary Device ID: 00841517101145
• NIH Device Record Key: 7e4796c8-96bd-4c51-9afb-438bb724d864
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: P21xp/5-1 MHz
• Version Model Number: P14563-20A
• 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: 1-877-657-8118
• Email: ffss-service@fujifilm.com

Operating and Storage Conditions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841517101145 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K152209

FDA Product Code

• ITX: Transducer, ultrasonic, diagnostic

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: 2016-09-15

On-Brand Devices [P21xp/5-1 MHz]

• 00841517101145: Diagnostic Ultrasound Transducer
• 00841517101138: Diagnostic Ultrasound Transducer
• 00841517106119: Diagnostic Ultrasound Transducer
• 00841517107024: Diagnostic Ultrasound Transducer
• 00841517109516: Diagnostic Ultrasound Transducer