Primary Device ID | 00840682140935 |
NIH Device Record Key | f9915dac-fd26-481e-9efd-55e004460e43 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | N/A |
Version Model Number | B1X5-F2 |
Company DUNS | 006580799 |
Company Name | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, INC. |
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 | false |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682140935 [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 | 2 |
Public Version Date | 2021-03-01 |
Device Publish Date | 2020-11-16 |