10,000 results
·
61ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
NIMBUS II PLUS AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 9, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PLUS AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 8, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
The Fresenius APD Luer-Lock Adapter, Catalog number 050-95018, is designed to connect a peritoneal dialysis bag equipped with a luer-lock connector to a Fresenius Automated Peritoneal Dialysis (APD) cycler set that uses the Fresenius Safe-Lock¿ connector (e.g., Liberty¿ cycler, Newton IQO cycler).
FDA Enforcement
Class II
·Terminated·Fresenius Medical Care Holdings, Inc.·July 28, 2021
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
NIMBUS II PAINPRO AMBULATORY INFUSION PUMP
FDA Adverse Event
Malfunction
·INFUTRONIX, LLC·Product code FRN·April 11, 2024
HYBRID GLENOID TRIAL PS 4MM LARGE
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code IQO·May 17, 2010
*
FDA Adverse Event
Malfunction
·SMITH & NEPHEW RICHARD, INC.·Product code IQO·March 5, 2004
HYBRID GLENOID INSTRUMENT DRILL GUIDE ALIGNMENT PIN
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code IQO·June 19, 2012
VANGUARD UNV 5IN1 TIBIAL TRIAL 71/75X10
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code IQO·April 20, 2012
COMPREHENSIVE INSTRUMENTION HUMERAL TRIAL 44MM STANDARD - 36MM STANDARD
FDA Adverse Event
Injury
·BIOMET ORTHOPEDICS·Product code IQO·April 3, 2012