SonoSite X-Porte P16055

GUDID 00841517103392

SonoSite X-Porte

FUJIFILM SONOSITE, INC.

General-purpose ultrasound imaging system
Primary Device ID00841517103392
NIH Device Record Key45fbd84a-4e6e-4cd2-a1ea-80bb4a5ffdda
Commercial Distribution StatusIn Commercial Distribution
Brand NameSonoSite X-Porte
Version Model NumberP16055-70
Catalog NumberP16055
Company DUNS014438860
Company NameFUJIFILM SONOSITE, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

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

Operating and Storage Conditions

Storage Environment HumidityBetween 15 Percent (%) Relative Humidity and 95 Percent (%) Relative Humidity

Device Identifiers

Device Issuing AgencyDevice ID
GS100841517103392 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

IYOSystem, imaging, pulsed echo, ultrasonic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2018-07-06
Device Publish Date2018-01-11

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00841517104733P19220-77
00841517104436P19220-75
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00841517103408P19220-20
00841517103392SonoSite X-Porte
00841517103385SonoSite X-Porte
00841517102821P17880-54
00841517102814P17880-11
00841517102807P17880-10
00841517102760P19220-55 
00841517102753P19220-10 
00841517102746P19220-05 
00841517102715P16055-60
00841517102708P16055-56
00841517102692P16055-35
00841517102685P16055-32
00841517101916P19220-65
00841517101909P19220-15
00841517100933P19220-60
00841517100926P17880-55
00841517104412P19220-21
00841517107420P20431-03

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