27 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Symetrex LTHD Catheter, Symetrex LTHD Catheter with Sideholes
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112755·BARRON VACUUM PUNCH 7.5MM
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112618·BARRON CORNEAL PUNCH 7.5MM
Tissue Holder
FDA UDI
KATENA PRODUCTS, INC.·00841668111192·STEEL BASE FOR BARRON AAC
ORION DIAGNOSTICA ULTRASENSITIVE CRP KIT, MODEL 68025, & ORION DIAGNOSTICA ULTRASENSITIVE CRP CONTROL, MODEL 68257
FDA 510(k)
FDA Class 2
·Immunology
NON-STERILE POWDER FREE PINEAPPLE SCENTED LATEX EXAMINATION GLOVES WITH PROTEIN CONTENT LABELING CLAIM (50 MICROGRAMS LE
FDA 510(k)
FDA Class 1
·General Hospital
LIFEVEST WCD 4000 SYSTEM
FDA Adverse Event
Malfunction
·ZOLL MANUFACTURING CORPORATION·Product code MVK·October 6, 2022
ENDURANT STENT GRAFT
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MIH·December 15, 2021
TALENT - UNK
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·January 5, 2022
UNK-CV-SR
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·February 16, 2022
VALIANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·January 5, 2022
ENDURANT STENT GRAFT
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code MIH·December 15, 2021
TALENT - UNK
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·January 5, 2022
ENDURANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·December 15, 2021
HEMOCUE GLUCOSE 201 MICROCUVETTES
FDA Adverse Event
Malfunction
·HEMOCUE AB·Product code CGA·June 28, 2013
TENDRIL ST
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC. CRMD·Product code NVN·January 13, 2014
ENRHYTHM DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code DXY·August 11, 2011
UNK-CV-SR
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·February 16, 2022
VALIANT STENT GRAFT
FDA Adverse Event
Injury
·MEDTRONIC IRELAND·Product code MIH·January 5, 2022
HEARTMATE 3 LVAS IMPLANT KIT
FDA Adverse Event
Injury
·THORATEC CORPORATION·Product code DSQ·April 13, 2021