KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS
FDA product code MAQ · Class 3 · 7 devices · 40 reports · 3 devices named in recalls
- BD COR™ GX INSTRUMENT 443990Becton, Dickinson And Company · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS1 recall22 reports
- BD COR™ PX INSTRUMENT 443988Becton, Dickinson And Company · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS1 recall4 reports
- Alinity m 09N15-095Abbott Molecular Inc. · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS1 recall0 reports
- BD Onclarity™ HPV Assay Reagent Pack 441990Becton, Dickinson And Company · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS8 reports
- BD Onclarity™ HPV SurePath™ Diluent Tubes 445329Becton, Dickinson And Company · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS3 reports
- BD Onclarity™ HPV Assay Reagent Pack 444075Becton, Dickinson And Company · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS2 reports
- cobas HPV 09040544190Roche Molecular Systems, Inc. · KIT, DNA DETECTION, HUMAN PAPILLOMAVIRUS1 report