346 results
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21ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ARCHON ANTERIOR CERVICAL PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
EVONOS
FDA UDI
Gyrus ACMI, LLC·00821925018532·CUPPED FORCEPS CURVED LEFT
MSI Precision Specialty Instruments
FDA UDI
Med Saver, Inc.·00194613052737·White Nylon Tube Brushes, 8 Fr, Brush Diameter ...
CaviCide
FDA UDI
METREX RESEARCH, LLC·00615375005330·Surface Disinfectant Decontaminant Cleaner
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311310250·
TALOS° HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321310250·
ihcDirect® Podoplanin Ab Conjugate 5mL
FDA UDI
NOVODIAX, INC.·00850030934413·Clone C125
ihcDirect® Podoplanin Ab
FDA UDI
NOVODIAX, INC.·00850000596337·Clone C125
ihcDirect® Podoplanin Ab
FDA UDI
NOVODIAX, INC.·00850000596320·Clone C125
ihcDirect® Podoplanin Ab Conjugate 15mL
FDA UDI
NOVODIAX, INC.·00850030934420·Clone C125
YA HORNG BLOOD PRESSURE MONITOR, YA HORNG BLOOD PRESSURE MONITOR, BLUETOOTH TRANSMISSION
FDA 510(k)
FDA Class 2
·Cardiovascular
TRIGEN LOW PROFILE BONE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
FEP
FDA UDI
Merit Medical Systems, Inc.·00884450000694·
FEP
FDA UDI
Merit Medical Systems, Inc.·00884450000656·
FEP
FDA UDI
Merit Medical Systems, Inc.·00884450000670·
FEP
FDA UDI
Merit Medical Systems, Inc.·00884450000663·
FEP
FDA UDI
Merit Medical Systems, Inc.·00884450000687·
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017
PENTAX
FDA Adverse Event
Injury
·PENTAX·Product code EOQ·January 10, 2017