CX Cart Diamond Select

GUDID 00884838107137

Philips Ultrasound, Inc.

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Primary Device ID00884838107137
NIH Device Record Keyabc16581-5a7e-4561-8a75-80693db3c817
Commercial Distribution StatusIn Commercial Distribution
Brand NameCX Cart Diamond Select
Version Model Number989606714631
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
GS100884838107137 [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 Date2021-04-05
Device Publish Date2021-03-27

Devices Manufactured by Philips Ultrasound, Inc.

00884838114203 - EPIQ 7 Diagnostic Ultrasound System Circular Edition2024-04-18 10.0.X Circular Edition
00884838114210 - EPIQ 5 Diagnostic Ultrasound System Circular Edition2024-04-18 10.0.X Circular Edition
00884838114227 - EPIQ CVx Diagnostic Ultrasound System Circular Edition2024-04-18 10.0.X Circular Edition
00884838114234 - EPIQ Elite Diagnostic Ultrasound System Circular Edition2024-04-18 10.0.X Circular Edition
00884838102729 - Transducer X11-4t2024-04-11
00884838115323 - QLAB Advanced Quantification Software2024-04-11
00884838122116 - Lumify Diagnostic Ultrasound System2024-04-08 Android 5.0
00884838120266 - Lumify Diagnostic Ultrasound System iOS2023-08-08 Release 5.0 iOS

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