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S102 P37,BED EXIT,72",10&11 SHORT,NO FS

FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828192316·S102 P3701,BED EXIT,72",10&11 SHORT,NO FAIL-SAF...

VERSACARE

FDA Adverse Event
Malfunction ·HILL-ROM RITTER·Product code FNL·August 14, 2008

ProPlan CMF Anatomical Model, Maxilla-Cranium, Clear Identification number SD900.208

FDA Recall
Completed ·Materialise USA LLC·Product code HWT·July 13, 2022

BRAINLAB Curve; Model/catalogue (article) numbers for Curve: 19901; 19901B; 19900; 19905 UDI (GTIN) for Curve: 04056481138011

FDA Enforcement
Class II ·Terminated·Brainlab AG·August 19, 2020

BRAINLAB Kick 2; Model/catalogue (article) numbers for Kick: 18170; 18070 UDI (GTIN) for Kick: 04056481006655

FDA Enforcement
Class II ·Terminated·Brainlab AG·August 19, 2020

NOBELACTIVE INTERNAL NP 3.5X13MM

FDA Adverse Event
Injury ·NOBEL BIOCARE USA INC·Product code DZE·October 21, 2024

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·October 27, 2011

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 22, 2010

ACRYSOF

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·September 22, 2010

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 5, 2013

SYBRALLOY CAPSULES

FDA Adverse Event
Malfunction ·KERR MFG CO.·Product code EJJ·January 12, 1994

SYNCHRONY III

FDA Adverse Event
Malfunction ·PACESETTER INC.·Product code DXY·February 6, 1998

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON MANUFACTURING, LTD. / HUNTINGTON·Product code HQL·May 21, 2013

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·May 21, 2013

ACRYSOF IQ TORIC

FDA Adverse Event
Other ·ALCON RESEARCH. LTD. / HUNTINGTON·Product code HQL·March 23, 2011

TRISTAR

FDA Adverse Event
Injury ·ETHICON ENDO-SURGERY, INC./A JOHNSON & JOHNSON G.·Product code GCJ·February 2, 1998

ACRYSOF RESTOR

FDA Adverse Event
Injury ·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·June 5, 2013

SECURE 3 MED/SURG BED

FDA Adverse Event
Malfunction ·STRYKER MEDICAL·Product code FNL·July 3, 2012

CAREFUSION PLEURX KIT

FDA Adverse Event
Injury ·CAREFUSION·Product code DWM·December 3, 2013

OPTIMA MP

FDA Adverse Event
Injury ·TELECTRONICS PACING SYSTEMS INC·Product code DXY·February 6, 1998