18 results · 38ms · Sources: EU EUDAMED, US FDA

Get notified when this changes

We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

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

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

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

ACCENT DR RF

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

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

GUARDIAN REAL-TIME MONITIOR

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code MDS·February 1, 2013

ADULT INSPIRATORY HEATED BREATHING CIRCUIT

FDA Adverse Event
Malfunction ·FISHER & PAYKEL HEALTHCARE LIMITED·Product code BTT·December 28, 2010

OT PING METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 17, 2014

TENDRIL ST

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

SIG C/R POROCOAT FEM LT SZ 3

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code MBH·April 8, 2009

DEPUY CMW 2 20G

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code LOD·November 5, 2019