216 results
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34ms
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Sources: EU EUDAMED, US FDA
Acuitas
FDA UDI
Opgen, Inc.·10812125010058·Approximately 700 µl Master Mix in 1.5 ml screw...
Acuitas
FDA UDI
Opgen, Inc.·20812125010031·A reagent kit for use with Acuitas AMR Gene Pan...
Acuitas
FDA UDI
Opgen, Inc.·20812125010086·Labeled, OpGen branded flash drive containing I...
Acuitas
FDA UDI
Opgen, Inc.·01812125010036·A reagent kit for use with Acuitas AMR Gene Pan...
Acuitas
FDA UDI
Opgen, Inc.·01812125010005·PCR Assay Plate Kit for use with Acuitas AMR Ge...
Acuitas
FDA UDI
Opgen, Inc.·10812125010027·PCR Plate Seal Package component of KT03U01-1 A...
Acuitas
FDA UDI
Opgen, Inc.·00812125010044·Assay Control is used to monitor extraction eff...
Acuitas
FDA UDI
Opgen, Inc.·20812125010062·QuantStudio Real-Time PCR Instrument Qualified ...
Acuitas
FDA UDI
Opgen, Inc.·01812125010081·Labeled, OpGen branded flash drive containing I...
Acuitas
FDA UDI
Opgen, Inc.·01812125010067·QuantStudio Real-Time PCR Instrument Qualified ...
Acuitas
FDA UDI
Opgen, Inc.·00812125010013·Sealed, 96-well plate in Mylar Pouch. Each sea...
Acuitas
FDA UDI
Opgen, Inc.·20812125010000·PCR Assay Plate Kit for use with Acuitas AMR Ge...
Acuitas
FDA UDI
Opgen, Inc.·10812125010041·Assay Control is used to monitor extraction eff...
Acuitas
FDA UDI
Opgen, Inc.·00812125010020·PCR Plate Seal Package component of KT03U01-1 A...
Acuitas
FDA UDI
Opgen, Inc.·20812125010079·QIAGEN EZ1 Advanced XL Instrument for use with ...
Acuitas
FDA UDI
Opgen, Inc.·00812125010051·Approximately 700 µl Master Mix in 1.5 ml screw...
Acuitas
FDA UDI
Opgen, Inc.·10812125010010·Sealed, 96-well plate in Mylar Pouch. Each sea...
Acuitas
FDA UDI
Opgen, Inc.·01812125010074·QIAGEN EZ1 Advanced XL Instrument for use with ...
GORE® CARDIOFORM SEPTAL OCCLUDER
FDA Adverse Event
Injury
·W. L. GORE & ASSOCIATES, INC.·Product code MLV·July 12, 2023
AdvanDx QuickFISH Slides, a component of the QuickFish BC Fixation Kit - BC, REF QFFIXBC1-25, Catalog Number: CS012 Control slides included as a component of the QFFIXBC1-25. The slides will provide non-fluorescent, wettable surface with dimensions appropriate for testing samples with QuickFISH BC culture identification kits.
FDA Recall
Terminated
·Opgen Inc·Product code LJG·May 14, 2018