Primary Device ID | 30014613312024 |
NIH Device Record Key | aab63298-b2df-4848-9c07-25a65dd96b91 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AmpliVue |
Version Model Number | GBS Assay |
Catalog Number | M202 |
Company DUNS | 079509836 |
Company Name | QUIDEL 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 | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 30014613312024 [Primary] |
NJR | Nucleic acid amplification assay system, group b streptococcus, direct specimen test |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2018-10-01 |
Device Publish Date | 2018-08-30 |
30014613312123 | AmpliVue GAS Assay |
30014613312116 | AmpliVue Trichomonas Assay |
30014613312109 | AmpliVue HSV 1+2 Assay |
30014613312093 | AmpliVue Bordetella Assay |
30014613312024 | AmpliVue GBS Assay |
30014613312017 | AmpliVue CDiff Assay |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
AMPLIVUE 85140233 4147342 Live/Registered |
Quidel Corporation 2010-09-28 |