Primary Device ID | 00884838076532 |
NIH Device Record Key | 3950e96c-d978-4cde-87ba-351c3bcfa24b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | IntelliVue Patient Monitor XG50 |
Version Model Number | 866063 |
Catalog Number | 866063 |
Company DUNS | 314101143 |
Company Name | Philips Medizin Systeme Böblingen GmbH |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Unsafe |
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 |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
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Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838076532 [Primary] |
MHX | MONITOR, PHYSIOLOGICAL, PATIENT(WITH ARRHYTHMIA DETECTION OR ALARMS) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-01-23 |
00884838120563 - MR Patient Care Kit, Sample, Agents, 3160 | 2025-05-29 KIT,SAMPLE,AGENTS,3160 |
00884838117839 - MR Patient Care Single Patch ECG Electrodes (25) | 2025-05-29 QUADTRODE MRI ECG PAD,25/BOX |
00884838117846 - MR Patient Care Multiple Patch ECG Electrodes (25) | 2025-05-29 ELECTRODE, MRI ECG, QUADTRODE CV, 25/BOX |
00884838117853 - MR Patient Care Neonatal ECG Electrodes (25) | 2025-05-29 ELECTRODE, NEONATE MRI ECG, QUADTRODE CV, 25/BOX |
00884838120532 - MR Patient Care Short Wide ECG 2.0 Cable AAMI | 2025-05-28 CAB,4 LD,CV MRI ECG,3160 |
00884838120549 - MR Patient Care Short Standard ECG 2.0 Cable AAMI | 2025-05-28 CAB,4 LD,MRI ECG,3160 |
00884838120693 - MR Patient Care Long Wide ECG 2.0 Cable AAMI | 2025-05-28 ECG Leadwire Set designed for use with the Expression MRI Patient Monitor when utlizing the system's Advanced ECG Gradient Filte |
00884838120730 - MR Patient Care Long Extra Wide ECG 2.0 Cable AAMI | 2025-05-28 Advanced Apps ECG Cable for wireless ECG modules |