14 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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SuperBall-RC
FDA 510(k)
FDA Class 2
·Orthopedic
3D Printed Interbody Systems
FDA UDI
Seaspine Orthopedics Corporation·10889981306328·Lateral Implant, 23mm x 14mm x 40mm, 15 Deg, 3D
REEF L
FDA UDI
Seaspine Orthopedics Corporation·10889981329037·LATERAL IMPLANT, REEF STERILE ASSY 23mm X 14mm ...
Reef L
FDA UDI
Seaspine Orthopedics Corporation·10889981426477·LATERAL IMPLANT, 23mm X 14mm X 40mm, 15°
Symmetry Gelpi
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00887482061565·Symmetry® Retractor, Gelpi, 4 1/2 in
Insignia
FDA UDI
ALPHATEC SPINE, INC.·00190376264677·4.0mm Fixed Angle, Self Drilling Screw, Dual Le...
Caphosol® Artifical Saliva (32 doses sachet box)
FDA 510(k)
FDA Unclassified
·Unknown
Palm NRG cellulite body device (model: Palm NRG body device)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
FT4, FREE THYROXINE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code CEC·February 2, 2015
BD VACUTAINER® SERUM BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO., (BD)·Product code JKA·June 2, 2023
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·November 11, 2014
CAPIOX RX OXYGENATOR W/HS RESERVOIR
FDA Adverse Event
TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTZ·September 7, 2011
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 24, 2013
SPINNING SPIROS® CLOSED MALE LUER
FDA Adverse Event
Malfunction
·ICU MEDICAL DE MEXICO, S. DE R.L. DE C.V.·Product code FPA·March 21, 2019