Primary Device ID | 10888234100836 |
NIH Device Record Key | 4a6dd7f7-17eb-48ea-b4c6-b9f7144304cc |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Filled Vial,Negative Control 1mL |
Version Model Number | 800-00287 |
Catalog Number | 800-00287 |
Company DUNS | 949103725 |
Company Name | BIOARRAY SOLUTIONS LTD |
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 | false |
Manufacturing Date | false |
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 -80 Degrees Celsius and -20 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10888234100836 [Primary] |
PEP | Molecular Erythrocyte Typing Test |
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 | 2014-09-24 |
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