82 results
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27ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BEAR and BEAR mini
FDA 510(k)
FDA Class 2
·Neurology
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526159785·PROTECT.LEVA ANKLE SUPPORT GRAY III
Bradshaw Medical Inc.
FDA UDI
Bradshaw Medical, Inc.·00810019930645·BIT, CRUCIFORM 4.0MM AO
Histofluor® Rodent LKS Fluorescent Antibody Test System
FDA UDI
IMMUNO CONCEPTS INC·M7491200803101·Rat LKS 8 Well Tissue Slides - 10 Slides
OLYMPUS FLUSHING PUMP OFP MODEL: OFP-1
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CEFAR MEDICAL AB CEFAR PRIMO
FDA 510(k)
FDA Class 2
·Neurology
Widex
FDA UDI
Widex A/S·05706069735536·Widex BEYOND B-F2 (Warm beige S-330 ) Telecoil,...
UNK - IOL
FDA Adverse Event
Other
·ALCON RESEARCH, LTD.·Product code HQL·April 17, 2008
ACRYSOF
FDA Adverse Event
Malfunction
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·April 16, 2008
UNK--IOL
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·March 21, 2008
UNK--IOL
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./ HUNTINGTON·Product code HQL·March 28, 2008
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD / HUNTINGTON·Product code HQL·March 27, 2008
CD HORIZON SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC.·Product code KWP·September 14, 2011
TIBIAL NAIL, STANDARD 10X390MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code JDS·July 8, 2008
FEMORAL NAIL, A/R 11X320 MM
FDA Adverse Event
Malfunction
·STRYKER OSTEOSYNTHESIS KIEL·Product code JDS·July 16, 2008
CAPSUREFIXNOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·June 8, 2013
ACRYSOF RESTOR
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·April 4, 2008
ACRYSOF
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code HQL·April 18, 2008
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON RESEARCH, LTD./HUNTINGTON·Product code MFK·April 10, 2008
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·November 26, 2020