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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