Primary Device ID | 00050428265109 |
NIH Device Record Key | bd119f4a-b0e9-4e60-aec1-74c65ebe678e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CVS Glucose Meter |
Version Model Number | 8000-10753 |
Company DUNS | 062312574 |
Company Name | WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
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 | true |
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 | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00050428265109 [Package] Contains: 10050428265106 Package: Carton [1 Units] In Commercial Distribution |
GS1 | 10050428265106 [Primary] |
GS1 | 10050428450991 [Previous] |
GS1 | 20050428265103 [Package] Package: Shipper [12 Units] In Commercial Distribution |
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 | 2021-03-30 |
Device Publish Date | 2021-03-22 |
10050428450991 | Advanced ProHealth Blood Glucose Meter, CVS 22L12 |
00050428265109 | Advanced ProHealth Blood Glucose Meter, CVS |