22 results · 24ms · Sources: EU EUDAMED, US FDA

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SPEED ARC

FDA 510(k)
FDA Class 2 ·Orthopedic

VACCESS LT LONG-TERM HEMODIALYSIS CATHETER PLUS

FDA UDI
Bard Access Systems, Inc.·00801741010880·VACCESS PLUS, ST, 16 FR. 27cm

Lippy

FDA UDI
MEDTRONIC XOMED, INC.·00681490034630·PROSTHESIS 1133270 LIPPY CUP PSTN .6X6.0

ABCFlex™, ABC®

FDA UDI
Conmed Corporation·30653405037884·ABCFlex™, ABC® Flexible Endoscopy Probe 2.3 mm ...

NOVOSCI READY SYSTEM, MODEL RS-200

FDA 510(k)
FDA Class 2 ·Cardiovascular

INSTINCT JAVA SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

FDA Adverse Event
Malfunction ·TANDEM DIABETES CARE·Product code QFG·October 12, 2022

ACTIV.A.C.¿ THERAPY SYSTEM

FDA Adverse Event
Injury ·KINETIC CONCEPTS, INC.·Product code OMP·February 12, 2018

SET, ADMINISTRATION, FOR PERITONEAL DIALYSIS, DISPOSABLE

FDA Adverse Event
Injury ·BAXTER HEALTHCARE - SWINFORD·Product code KDJ·October 1, 2014

INFUSE BONE GRAFT

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 29, 2013

ION PACLITAXEL-ELUTING PLATINUM CHROMIUM CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·June 20, 2011

ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM

FDA Adverse Event
Injury ·KINETIC CONCEPTS, INC.·Product code OMP·June 8, 2021

ACTIV.A.C. ION PROGRESS REMOTE THERAPY MONITORING SYSTEM

FDA Adverse Event
Injury ·KINETIC CONCEPTS, INC.·Product code OMP·July 14, 2021

INSTINCT JAVA SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code MNH·October 30, 2019

INSTINCT JAVA SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code MNH·October 30, 2019

INSTINCT JAVA SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code MNH·October 30, 2019

INSTINCT JAVA ROD, UNKNOWN

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code MNH·October 30, 2019

INSTINCT JAVA ROD, UNKNOWN

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code MNH·October 31, 2019

INSTINCT JAVA SCREW, UNKNOWN SIZE

FDA Adverse Event
Injury ·ZIMMER SPINE·Product code MNH·October 31, 2019

ABC GI PROBE 2.3MM X 270CM

FDA Adverse Event
Malfunction ·CONMED CORPORATION·Product code GEI·March 25, 2020