EPIQ Elite Diamond Select Ultrasound

GUDID 00884838109971

To support the 7.x software version

Philips Ultrasound, Inc.

General-purpose ultrasound imaging system
Primary Device ID00884838109971
NIH Device Record Key004acf02-f82c-43c3-bcef-3b9a04865e5f
Commercial Distribution StatusIn Commercial Distribution
Brand NameEPIQ Elite Diamond Select Ultrasound
Version Model Number795125
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 Batchfalse
Serial Numbertrue
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
GS100884838109971 [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 Date2022-02-28
Device Publish Date2022-02-18

Devices Manufactured by Philips Ultrasound, Inc.

00884838122277 - QLAB Advanced Quantification Software2024-06-06 VM11.0 update
00884838123960 - EPIQ CVx Diagnostic Ultrasound System2024-06-06 VM11.0 Update
00884838123977 - EPIQ CVxi Diagnostic Ultrasound System2024-06-06 VM 11.0 Update
00884838123984 - Affiniti CVx Diagnostic Ultrasound System2024-06-06 VM11.0 update
00884838114265 - Affinti 30 Diagnostic Ultrasound System Circular Edition2024-06-04 VM10.0 Update
00884838114241 - Affinti 50 Diaagnostic Ultrasound System Circular Edition2024-05-13 Software Version 10.0.2
00884838114258 - Affinti 70 Diaagnostic Ultrasound System Circular Edition2024-05-13 Software Version 10.0.2
00884838114203 - EPIQ 7 Diagnostic Ultrasound System Circular Edition2024-04-18 10.0.X Circular Edition

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