14 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PRECICE Bone Transport System
FDA 510(k)
FDA Class 2
·Orthopedic
ECHO BI-METRIC MICROPLASTY HIP SYSTEM
FDA UDI
Biomet Orthopedics, LLC·00880304697836·
OsteoMed
FDA UDI
OSTEOMED LLC·00845694009812·3.0mm x 16mm Cannulated Lag Screw
CETRA
FDA UDI
Orthofix US LLC·18257200120765·4.0MM X 16MM PRIMARY CONSTRAINED SELF-TAPPING S...
OsteoMed
FDA UDI
OSTEOMED LLC·00845694071109·Cannulated 3.0 x 16mm Lag Screw Sterile Qty 5
WARMTOUCH COMPACT WARMING UNIT
FDA Adverse Event
Malfunction
·COVIDIEN/FORMERLY TYCO·Product code DWJ·December 23, 2010
VERI-Q SELF-TESTING AND VERI-Q PLUS MGD-2001 BLOOD GLUCOSE MONITORING SYSTEMS
FDA 510(k)
FDA Class 2
·Clinical Chemistry
VITAL SIGNS MONITOR
FDA 510(k)
FDA Class 2
·Cardiovascular
WARM TOUCH II COMPACT WARMING UNIT
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY TYCO HEALTHCARE·Product code DWJ·September 24, 2010
Versa-Fx®
FDA UDI
Zimmer, Inc.·00889024036390·
VASOVIEW HEMOPRO 2 EVH SYSTEM
FDA Adverse Event
Malfunction
·MAQUET CARDIOVASCULAR, LLC·Product code GEI·July 21, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE. LTD.·Product code FRN·October 13, 2008
OBTRYX SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·June 27, 2013
Olympus Sterile Optical Laser Fiber, single use and reusable
FDA Enforcement
Class II
·Terminated·Quanta System, S.p.A.·June 16, 2021