94 results
·
27ms
·
Sources: EU EUDAMED, US FDA
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·MICROVEL(R) WITH HEMASHIELD
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·MICROVEL(R) WITH HEMASHIELD
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD WOVEN DOUBLE VELOUR GRAFTS 7MMX100CM
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD ETS(TM) FLANGED GRAFT
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD(R) WOVEN DOUBLE VELOUR GRAFT
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD WOVEN DOUBLE VELOUR GRAFTS 7MMX100CM
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD WOVEN DOUBLE VELOUR GRAFTS
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD WOVEN DOUBLE VELOUR GRAFTS
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD(R) MICROVEL (R) DOUBLE VELOUR GRAFT
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD WOVEN DOUBLE VELOUR GRAFTS
FDA Pre-Market Approval
HEMASHIELD (R) MICROVEL (R) DOUBLE VELOUR
Prosthesis, Vascular Graft, Of 6mm And Greater Diameter
FDA Pre-Market Approval
FDA Class 2
·HEMASHIELD WOVEN DOUBLE VELOUR GRAFTS 12 X 6MM
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·00842209122769·
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
STRIPS
FDA 510(k)
FDA Class 1
·Microbiology
NUCLEUS 22
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·May 18, 2025
Lens, Contact, Orthokeratology, Overnight
FDA Pre-Market Approval
FDA Class 3
·Euclid Orthokeratology (oprifocon A) Contact Lenses for Overnight Wear and Euclid Orthokeratology (tisilfocon A) Contact
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·Restylane Refyne, Restylane Defyne
PRECISION SPECTRA®
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·May 30, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 20, 2012