Primary Device ID | 00389154000631 |
NIH Device Record Key | 20373c2d-cba4-4269-aa21-d2f832395684 |
Commercial Distribution Discontinuation | 2016-12-09 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | GL GoodLife AC-302 Blood Glucose Monitoring System |
Version Model Number | AC-11 AC302 |
Catalog Number | 3K-01-16003R |
Company DUNS | 658644174 |
Company Name | HMD BIOMEDICAL INC. |
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 | true |
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 | 00389154000631 [Primary] |
GS1 | 00389154000648 [Package] Package: [60 Units] Discontinued: 2016-12-09 Not in Commercial Distribution |
LFR | Glucose Dehydrogenase, Glucose |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-12-09 |
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