19 results · 23ms · Sources: EU EUDAMED, US FDA

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Decanting Device

FDA 510(k)
FDA Class 2 ·General Hospital

DERMATOLOGIC TREATMENT SYSTEM (DTS) G2

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

6000CMS

FDA Adverse Event
Malfunction ·MOOG DEVICE GROUP·Product code FRN·June 11, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·July 28, 2011

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 17, 2014

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 29, 2020

DYB INTRODUCER, CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code DYB·November 12, 2025

FLEXOR SHUTTLE SELECT GUIDING SHEATH

FDA Adverse Event
Injury ·COOK INC·Product code DYB·October 29, 2025

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·January 12, 2018

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·April 19, 2021

UNKNOWN

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 15, 2020

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·January 16, 2020

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·August 15, 2019

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·December 4, 2019

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·September 12, 2019

FLEXOR SHUTTLE TIBIAL GUIDING SHEATH

FDA Adverse Event
Malfunction ·COOK INC·Product code DYB·October 10, 2019