27 results · 23ms · Sources: EU EUDAMED, 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