25 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ESTEEM STERILE POLYISOPRENE SURGICAL GLOVES
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526780736·LEVAMED ACTIVE ANKLE SUP SLVR L I
Henry Schein
FDA UDI
HENRY SCHEIN, INC.·00304040011584·Zirlux 16+ A1 95X14
BUSCH®, BNA®
FDA UDI
BUSCH & CO. GmbH & Co. KG·D8120117211·Steel, cone flat, excavating bur
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033378861·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033378854·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033378885·
BETSEY JOHNSON
FDA UDI
FGX INTERNATIONAL INC.·00193033378878·
PASCO MIC AND MIC/ID PANELS
FDA 510(k)
FDA Class 2
·Microbiology
AXIOM ARTIS MODULAR ANGIOGRAPHY SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
BD VACUTAINER® SST¿ II ADVANCE PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·April 25, 2018
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194479868·4.5MM PROVISIONAL ROD
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194479974·VERTEGLIDE 4.5mm MANUAL COUNTER TORQUE TUBE
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194480086·VERTEGLIDE 4.5MM ROD BEND CHECKER
VerteGlide Spinal Growth Guidance System
FDA UDI
ORTHOPEDIATRICS CORP.·00840194480017·4.5 OPEN VERTEGLIDE PEDICLE SCREW DRIVER
XPS® BUR GUARD - VISAO®
FDA Adverse Event
Injury
·MEDTRONIC XOMED INC.·Product code ERL·April 22, 2016
XPS® BUR
FDA Adverse Event
Malfunction
·MEDTRONIC XOMED INC.·Product code EQJ·March 13, 2017
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·March 19, 2013
RSP SHOULDER
FDA Adverse Event
Other
·ENCORE MEDICAL, L.P.·Product code KWS·March 1, 2011
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·February 26, 2008