HFL50xp/15-6 MHz

GUDID 00841517101008

Diagnostic Ultrasound Transducer

FUJIFILM SONOSITE, INC.

Extracorporeal ultrasound imaging transducer, hand-held
Primary Device ID00841517101008
NIH Device Record Key4a8166ef-545f-49ac-aafa-1faa284d9ce3
Commercial Distribution StatusIn Commercial Distribution
Brand NameHFL50xp/15-6 MHz
Version Model NumberP14567-22A
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

Phone1-877-657-8118
Emailffss-service@fujifilm.com

Operating and Storage Conditions

Handling Environment Atmospheric PressureBetween 50 KiloPascal and 106 KiloPascal

Device Identifiers

Device Issuing AgencyDevice ID
GS100841517101008 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

ITXTransducer, ultrasonic, diagnostic

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 Date2016-09-15

On-Brand Devices [HFL50xp/15-6 MHz]

00841517102630Diagnostic Ultrasound Transducer
00841517101008Diagnostic Ultrasound Transducer
00841517100995Diagnostic Ultrasound Transducer
00841517106126Diagnostic Ultrasound Transducer
00841517107055Diagnostic Ultrasound Transducer
00841517107550P14567-20A
00841517109455Diagnostic Ultrasound Transducer

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.