Primary Device ID | 04719871820315 |
NIH Device Record Key | b57e17e7-45e2-475a-bc60-e729fffdb20f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NuvoMed |
Version Model Number | P5228 BGM-6/0352 |
Company DUNS | 658447255 |
Company Name | BIOTEST MEDICAL CORPORATION |
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 | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04719871820315 [Primary] |
NBW | System, Test, Blood Glucose, Over The Counter |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-04-09 |
Device Publish Date | 2018-03-07 |
04719871820322 | NuvoMed Wireless Glucose Monitor |
04719871820315 | NuvoMed Wireless Blood Glucose Monitoring System |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
NUVOMED 88404114 5896895 Live/Registered |
NUVOMED, INC. 2019-04-26 |
NUVOMED 87257013 5536506 Live/Registered |
NUVOMED, INC. 2016-12-05 |