Primary Device ID | 00840682108799 |
NIH Device Record Key | bf7b196e-c165-43ba-9a72-944a95999936 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ApexPro |
Version Model Number | 600 MHz Receiver |
Company DUNS | 784985108 |
Company Name | GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES, 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 | 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(800)558-5120 |
xx@xx.xx |
Storage Environment Humidity | Between 15 Percent (%) Relative Humidity and 97 Percent (%) Relative Humidity |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840682108799 [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 | 2016-06-10 |
00840682109024 | FH Transceiver |
00840682108928 | CH Transmitter |
00840682108799 | 600 MHz Receiver |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
APEXPRO 98560773 not registered Live/Pending |
Catalyst Energy Services LLC 2024-05-21 |
APEXPRO 97202355 not registered Live/Pending |
Catalyst Energy Services LLC 2022-01-04 |
APEXPRO 87232935 5586843 Live/Registered |
GILDAN BRANDED APPAREL SRL 2016-11-10 |
APEXPRO 86270644 not registered Dead/Abandoned |
DIGITCARE CORPORATION 2014-05-02 |
APEXPRO 78750571 3142255 Live/Registered |
General Electric Company 2005-11-09 |