1,667 results
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37ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UNKNOWN REVITAN-MODULAR FLUTED TAPERED STEM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·October 7, 2024
FUSION HOLLOW FIBER OXYGENATOR
FDA Adverse Event
Malfunction
·PERFUSION SYSTEMS·Product code DTZ·November 4, 2025
DAVINCI XI
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL, INC·Product code NAY·July 9, 2025
VENTRALIGHT ST W/ ECHO
FDA Adverse Event
Injury
·DAVOL INC., SUB. C.R. BARD, INC. -1213643·Product code FTL·November 3, 2021
EDWARDS PASCAL PRECISION
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NKM·March 29, 2023
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·November 21, 2023
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·November 21, 2023
UNKNOWN REVITAN-MODULAR FLUTED TAPERED STEM
FDA Adverse Event
Injury
·ZIMMER GMBH·Product code LZO·October 7, 2024
TRICLIP G4 SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NPS·December 6, 2024
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·November 21, 2023
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·March 19, 2026
MITRACLIP G4 CLIP DELIVERY SYSTEM
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code NKM·October 24, 2022
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·March 19, 2026
PERCEVAL PLUS SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·CORCYM S.R.L.·Product code LWR·September 19, 2022
TREO ABDOMINAL STENT-GRAFT SYSTEM
FDA Adverse Event
Injury
·BOLTON MEDICAL, INC.·Product code MIH·March 19, 2026
PERCEVAL SUTURELESS AORTIC HEART VALVE
FDA Adverse Event
Injury
·LIVANOVA CANADA CORP.·Product code LWR·April 3, 2016
AMPLATZER TALISMAN PFO OCCLUDER
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code MLV·January 15, 2025
Home Monitoring Ophthalmic Optical Coherence Tomography (Oct) Imaging Device
FDA classification
FDA Class 2
·Home Monitoring Ophthalmic Optical Coherence Tomography (Oct) Imaging Device
Bax RMab
FDA UDI
BIO SB, INC.·B502BSB60820·Bax is a rabbit monoclonal antibody derived fro...
Bax RMab
FDA UDI
BIO SB, INC.·B502BSB60810·Baxis a rabbit monoclonal antibody derived from...