Primary Device ID | 00884838064713 |
NIH Device Record Key | 583ca242-a8f4-4f78-940b-5530186cf94c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Lumify Ultrasound System |
Version Model Number | 989605449841 |
Company DUNS | 063377717 |
Company Name | Philips Ultrasound, Inc. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838064713 [Primary] |
IYN | System, imaging, pulsed doppler, ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-07-25 |
00884838122277 - QLAB Advanced Quantification Software | 2024-06-06 VM11.0 update |
00884838123960 - EPIQ CVx Diagnostic Ultrasound System | 2024-06-06 VM11.0 Update |
00884838123977 - EPIQ CVxi Diagnostic Ultrasound System | 2024-06-06 VM 11.0 Update |
00884838123984 - Affiniti CVx Diagnostic Ultrasound System | 2024-06-06 VM11.0 update |
00884838114265 - Affinti 30 Diagnostic Ultrasound System Circular Edition | 2024-06-04 VM10.0 Update |
00884838114241 - Affinti 50 Diaagnostic Ultrasound System Circular Edition | 2024-05-13 Software Version 10.0.2 |
00884838114258 - Affinti 70 Diaagnostic Ultrasound System Circular Edition | 2024-05-13 Software Version 10.0.2 |
00884838114203 - EPIQ 7 Diagnostic Ultrasound System Circular Edition | 2024-04-18 10.0.X Circular Edition |