2,707 results
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54ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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PDQ AND PDQ-TI ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
PDQ Platelet Centrifuge
FDA UDI
Bio/Data Corporation·G0561068421·
PDQ AMEBIASIS
FDA 510(k)
FDA Class 2
·Microbiology
Trinity Biotech
FDA UDI
PRIMUS CORPORATION·05391516748636·Hemoglobin A1c assay, PDQ Wash Reagent
NEU_INS_STIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·August 17, 2012
Trinity Biotech
FDA UDI
PRIMUS CORPORATION·05391516748629·Hemoglobin A1c assay, PDQ Diluent Reagent - 940mL
Trinity Biotech
FDA UDI
PRIMUS CORPORATION·05391516748612·Hemoglobin A1c assay, PDQ 2 Reagent - 940mL
STAY HARD
FDA UDI
Blush Novelties·00853858007000·Stay Hard - Donut Rings - 50 Piece PDQ Display
...
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·June 18, 2020
LEAD
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code MHY·June 18, 2020
LEAD
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 12, 2021
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Death
·MEDTRONIC NEUROMODULATION·Product code MHY·July 5, 2018
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·October 6, 2021
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·April 25, 2023
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·July 23, 2013
UNKNOWN IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·June 15, 2018
ELI380 ERGO WAM WLAN USB DICOM PDQ IEC B
FDA Adverse Event
Malfunction
·MORTARA INSTRUMENT·Product code DPS·November 30, 2020
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 7, 2011
ACTIVA
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·December 7, 2011
IMPLANTABLE NEUROSTIMULATOR
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code MHY·January 5, 2022