V9-2 Ultrasound Transducer

GUDID 00884838102606

Philips Ultrasound, Inc.

Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held Extracorporeal ultrasound imaging transducer, hand-held
Primary Device ID00884838102606
NIH Device Record Keyeac72214-8485-40d4-a052-44f1496a27e4
Commercial Distribution StatusIn Commercial Distribution
Brand NameV9-2 Ultrasound Transducer
Version Model Number989606717071
Company DUNS063377717
Company NamePhilips Ultrasound, 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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100884838102606 [Primary]

FDA Product Code

IYNSystem, imaging, pulsed doppler, ultrasonic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-12-23
Device Publish Date2020-12-15

Devices Manufactured by Philips Ultrasound, Inc.

00884838120266 - Lumify Diagnostic Ultrasound System iOS2023-08-08 Release 5.0 iOS
00884838121423 - TOMTEC ARENA2023-07-27
00088483810859 - Transducer mL26-82023-05-30
00884838114128 - EPIQ 5W Diagnostic Ultrasound System2023-05-18 Software version-10.0.X
00884838114111 - EPIQ 5 Diagnostic Ultrasound System2023-05-17 Software version-10.0.X
00884838114098 - EPIQ 7 Diagnostic Ultrasound System2023-05-12 Software version - 10.0.x
00884838114104 - EPIQ 7W Diagnostic Ultrasound System2023-05-12 Software version - 10.0.x
00884838114135 - EPIQ CVx Diagnostic Ultrasound System2023-05-12 Software version 10.0.X

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