Primary Device ID | 00884838028890 |
NIH Device Record Key | 0d903db3-8bb7-4d58-8744-bbf652bb2ec7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SureSigns VS4 |
Version Model Number | 863283 |
Catalog Number | 863283 |
Company DUNS | 078628040 |
Company Name | Philips Medical Systems |
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 |
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 | |
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 | |
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 | 00884838028890 [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 | 4 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2016-10-03 |
00884838087095 | 863283 |
00884838028890 | 863283 |
00884838091405 | 863379 |