Primary Device ID | 00884838064904 |
NIH Device Record Key | cdb93db0-0c0c-43ae-b490-6dbfda918f1b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PHILIPS IntelliVue MP2 Military |
Version Model Number | 867059 |
Catalog Number | 867059 |
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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
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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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884838064904 [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 | 2016-09-28 |
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