Primary Device ID | 00817980020078 |
NIH Device Record Key | dc91bc42-93e9-4d54-80df-84559c26e4f3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Vasomedical-Biox™ 2301 Combined 3 Channel ECG Holter & ABP Monitor |
Version Model Number | Model 2301 |
Catalog Number | A10-0085 |
Company DUNS | 197210248 |
Company Name | VASOMEDICAL, 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(516)508-5818 |
eohara@vasomedical.com | |
Phone | +1(516)508-5818 |
eohara@vasomedical.com |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Storage Environment Atmospheric Pressure | Between 50 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817980020078 [Primary] |
DSH | RECORDER, MAGNETIC TAPE, MEDICAL |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-11-29 |