Affiniti 50 Diamond Select Ultrasound System

GUDID 00884838106567

Philips Ultrasound, Inc.

General-purpose ultrasound imaging system
Primary Device ID00884838106567
NIH Device Record Key7ea11b29-1e1d-4213-8cde-1f56b8ec7a9d
Commercial Distribution StatusIn Commercial Distribution
Brand NameAffiniti 50 Diamond Select Ultrasound System
Version Model Number795118
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
GS100884838106567 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LLZSystem, Image Processing, Radiological

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-09-29
Device Publish Date2021-09-21

Devices Manufactured by Philips Ultrasound, Inc.

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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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