10,000 results
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272ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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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