25 results · 25ms · Sources: EU EUDAMED, US FDA

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CXI Support Catheter

FDA 510(k)
FDA Class 2 ·Cardiovascular

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·April 18, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 2, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 18, 2021

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·April 21, 2021

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·June 21, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·January 25, 2024

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·January 29, 2019

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 12, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·March 12, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·December 8, 2022

CXI SUPPORT CATHETER

FDA Adverse Event
Malfunction ·COOK INC·Product code KRA·March 31, 2022

CXI SUPPORT CATHETER

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

POWDER-FREE VINYL PATIENT EXAMINATION GLOVES

FDA 510(k)
FDA Class 1 ·General Hospital

STRYKER KNIFELIGHT

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

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN INC.·Product code NBW·July 13, 2011

SPRINT QUATTRO SECURE

FDA Adverse Event
Injury ·MPRI·Product code LWS·October 10, 2014

ADVANCED PATELLA 35MM 3 PEG IMPLANT

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code JWH·January 9, 2024

Artis zeego, Material no. 10280959 , for angiography and whole body radiographic/fluoroscopic procedures.

FDA Enforcement
Class II ·Terminated·Siemens Medical Solutions USA, Inc·July 4, 2018