SonoSite X-Porte P19220

GUDID 00841517103408

General-purpose ultrasound imaging system

Primary Device ID	00841517103408
NIH Device Record Key	5d367fd0-d1a6-4444-814d-337b98a645fb
Commercial Distribution Status	In Commercial Distribution
Brand Name	SonoSite X-Porte
Version Model Number	P19220-20
Catalog Number	P19220
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

Phone	+1(999)999-9999
Email	xyz@xyz.com

Handling Environment Humidity

Between 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Issuing Agency	Device ID
GS1	00841517103408 [Primary]

IYO	System, imaging, pulsed echo, ultrasonic

Steralize Prior To Use	false
Device Is Sterile	false