8 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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APR ACETABULAR INSERTS IOI BIPOLAR
FDA 510(k)
FDA Class 2
·Orthopedic
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515243323·Sickle knife, sharp, left, adult
PATIENT EXAM GLOVES(MFG: LIAONING MACHINERY)
FDA 510(k)
FDA Class 1
·General Hospital
GSI 38 AUTO TYMP
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
MAXPLUS NEEDLELESS CONNECTOR
FDA Adverse Event
Malfunction
·CAREFUSION CORP·Product code FPA·January 2, 2013
SPECTRUM INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 3, 2014
SYSTEM 6 ASEPTIC HOUSING ASSY
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·December 14, 2010
UHN Ø6.7 L240 TAN VIOL
FDA Adverse Event
Injury
·SYNTHES SALZBURG·Product code HSB·February 16, 2016