| Primary Device ID | 04053228000068 |
| NIH Device Record Key | 75f1bc22-79ca-442d-a782-9a26059787f7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | QIAamp DSP Virus Kit |
| Version Model Number | 1 |
| Catalog Number | 60704 |
| Company DUNS | 317103745 |
| Company Name | QIAGEN GmbH |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 04053228000068 [Primary] |
| JJH | Clinical Sample Concentrator |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2017-08-15 |
| 04053228035725 - therascreen® BRAF RGQ PCR Kit | 2025-06-09 The therascreen BRAF V600E RGQ PCR Kit is a real-time PCR test for the qualitative detection of V600E mutations in the BRAF gene |
| 04053228048381 - QIAstat-Dx® GI Panel 2 Mini B | 2025-04-07 |
| 04053228049166 - QIAstat-Dx® GI Panel 2 Mini B&V | 2025-02-26 |
| 04053228048862 - QIAstat-Dx® Respiratory Panel Mini | 2024-12-13 |
| 04053228003526 - QIAGEN Buffer ASL® | 2024-10-08 Stool Lysis Buffer |
| 04053228048268 - QIAsymphony® DSP Circulating DNA Maxi Kit (192) | 2024-10-08 |
| 04053228048350 - QIAsymphony® DSP Circulating DNA Kit (96) | 2024-10-08 |
| 04053228048770 - QIAcuityDx® Four | 2024-10-08 The QIAcuityDx® Four is an automated digital PCR (dPCR) instrument designed to perform amplification, detection (qualitative an |