Primary Device ID | 00856893004027 |
NIH Device Record Key | ab4294f5-482d-40e9-a961-bc01bbed8b39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Aggreguide |
Version Model Number | A-100 |
Catalog Number | 12020 |
Company DUNS | 078703793 |
Company Name | AGGREDYNE, 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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Storage Environment Temperature | Between 15 Degrees Celsius and 25 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00856893004027 [Primary] |
GS1 | 00856893004072 [Package] Package: Case [20 Units] In Commercial Distribution |
GS1 | 10856893004024 [Package] Package: Case [20 Units] In Commercial Distribution |
JOZ | System, Automated Platelet Aggregation |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-10-01 |
Device Publish Date | 2019-09-23 |
00856893004041 | Whole Blood Aggregometer |
00856893004027 | AggreDYNE A-100 ADP Assay |