Primary Device ID | 07540211000015 |
NIH Device Record Key | f128efaf-b826-4b43-b19c-0faedd7b1ab0 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BpTRU |
Version Model Number | BPM-100 |
Company DUNS | 203111315 |
Company Name | BpTRU Medical Devices, a div of |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 07540211000015 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-11-08 |
Device Publish Date | 2016-11-25 |
07540211000022 | BPM-200 |
07540211000015 | BPM-100 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() BPTRU 76315869 2676951 Live/Registered |
MFC INDUSTRIAL LTD. 2001-09-21 |