Primary Device ID | 00869876000046 |
NIH Device Record Key | 32f3a672-0432-4a85-bbfd-527acf5a16d9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | iBloodPressure |
Version Model Number | SMBP802-GS-002 |
Company DUNS | 117014140 |
Company Name | SMART METER LLC |
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 | 00869876000046 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-10-05 |
Device Publish Date | 2021-09-27 |
00869876000039 | iBloodPressure Cellular Blood Pressure Monitor, Adult, Large |
00869876000053 | iBloodPressure Cellular Blood Pressure Monitor, Adult, Large |
00869876000046 | iBloodPressure, Cellular, Blood Pressure Monitor |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
IBLOODPRESSURE 90090378 not registered Live/Pending |
Smart Meter LLC 2020-08-03 |
IBLOODPRESSURE 90088160 not registered Live/Pending |
Smart Meter LLC 2020-08-02 |