17 results · 23ms · Sources: EU EUDAMED, US FDA

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COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER SINGLE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL·Product code HQL·June 15, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·June 15, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIECE

FDA Adverse Event
Injury ·STAAR SURGICAL CO.·Product code HQL·June 21, 2006

COLLAMER ULTRAVIOLET-ABSORBING POSTERIOR CHAMBER THREE PIEC

FDA Adverse Event
Malfunction ·STAAR SURGICAL CO.·Product code HQL·June 23, 2006

TENDRIL STS

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 7, 2022

TENDRIL STS

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 7, 2022

ACCENT DR RF

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code LWP·November 19, 2015

ONETOUCHPING GLUCOSEMGMTSYSTEM

FDA Adverse Event
Malfunction ·ANIMAS CORPORATION·Product code LZG·March 5, 2013

MILD

FDA Adverse Event
Injury ·VERTOS MEDICAL·Product code HTX·February 9, 2011

SPRINT

FDA Adverse Event
Injury ·MPRI·Product code LWS·August 7, 2014

TENDRIL ST

FDA Adverse Event
Injury ·ST. JUDE MEDICAL, INC.(CRM-SYLMAR)·Product code NVN·December 10, 2018

ACUVUE ABILITI OVERNIGHT THERAPEUTIC LENSES FOR MYOPIA MANAGEMENT

FDA Adverse Event
Malfunction ·MENICON CO. LTD.·Product code NUU·January 2, 2024