61 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNK - CONSTRUCTS: PFNA-II
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HSB·July 15, 2021
UNK - CONSTRUCTS: PFNA
FDA Adverse Event
Injury
·SYNTHES GMBH·Product code HSB·March 7, 2021
INSULIN REPOSITORY
FDA Adverse Event
DISETRONIC MEDICAL SYSTEMS·Product code LZG·September 17, 1998
ENDOTAK DSP
FDA Adverse Event
Malfunction
·CARDIAC PACEMAKERS·Product code LWS·February 9, 2001
DURATA STS OPTIM
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2008
DURATA STS OPTIM ACTIVE FIXATION LEAD, DF-4 CONNECTO
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2012
GUGLIELMI DETACHABLE COIL- GDC-10
FDA Adverse Event
Malfunction
·TARGET THERAPEUTICS/A DIVISION OF BOSTON SCIENTIFIC CORP.·Product code HCG·March 16, 1999
SWEET TIP BIPOLAR LEAD
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code DXY·July 8, 1997
BIPOLAR STEROID ELUTING LEAD
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code DTB·May 8, 1997
INFLATABLE PENILE PROSTHESIS
FDA Adverse Event
Injury
·AMERICAN MEDICAL SYSTEMS, INC.·Product code FHW·January 2, 1997
ENDOTAK RELIANCE
FDA Adverse Event
Malfunction
·CPI - DEL CARIBE·Product code LWS·April 2, 2015
MOBILE STAND
FDA Adverse Event
Malfunction
·CRITIKON, DIV OF ETHICON, INC.·Product code DXN·July 10, 1998
PRECISION
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·June 11, 2009
ENDOTAK RELIANCE G
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS, INC·Product code LWS·August 9, 2006
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code OJX·April 11, 2013
SWEET TIP BIPOLAR LEAD
FDA Adverse Event
Injury
·CARDIAC PACEMAKERS·Product code DXY·March 6, 1997
IMPLANTABLE COLLAMER LENS (ICL)
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·March 23, 2024
IMPLANTABLE DEFIBRILLATOR/PACEMAKER/LEAD
FDA Adverse Event
CARDIAC PACEMAKERS, INC.·Product code LWS·January 31, 1996
ACCLAIM STANDARD TUBING DEVICE
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code FRN·April 17, 1998
TI MATRIXMIDFACE SCREW SELF-DRILLING 6MM
FDA Adverse Event
Malfunction
·SYNTHES MONUMENT·Product code DZL·April 27, 2017