| 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 |