10,000 results
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69ms
·
Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·VARIOUS FAMILIES OF CRT-ICD'S
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·VARIOUS FAMILIES OF PACEMAKERS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VARIOUS FAMILIES OF ICD'S
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·THE CLOSER AK 6 FR. SMC DEVICE
PROFEMUR XTR HIP STEM
FDA 510(k)
FDA Class 3
·Orthopedic
LEAD MODIFICATION
FDA 510(k)
FDA Class 3
·Cardiovascular
PM CEMENTLESS SCREW-IN ACETABULAR CUP
FDA 510(k)
FDA Class 3
·Orthopedic
BIPOLAR LEADS, DISP.
FDA 510(k)
FDA Class 3
·Cardiovascular
PULSTRON MODEL 100
FDA 510(k)
FDA Class 3
·Cardiovascular
IMPLANTABLE PULSE DEVICES
FDA 510(k)
FDA Class 3
·Cardiovascular
INTERMEDICS 430-07 BIPOL IMPLANT ENDOCARD PAC LEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
MODEL 493-03 PACING LEAD
FDA 510(k)
FDA Class 3
·Cardiovascular
PACEMAKER, ELECTRODE, PERMANENT & TEMP.
FDA 510(k)
FDA Class 3
·Cardiovascular
REVELATION STEM, MODEL 427-21/42-080/180
FDA 510(k)
FDA Class 3
·Orthopedic
DIRECTIONAL BOOT
FDA 510(k)
FDA Class 3
·Cardiovascular
SKINTACT PEDIATRIC MULTIFUNCTION ELECTRODES WITH DH03 GEL
FDA 510(k)
FDA Class 3
·Cardiovascular
DURA PADZ (REUSABLE ELECTRODE), DURA PADZ GEL (DISPOSABLE HYDROGEL) MODEL 8900-0300, 8900-0325
FDA 510(k)
FDA Class 3
·Cardiovascular
CARCIAC PULSE GENERATOR 254-20
FDA 510(k)
FDA Class 3
·Cardiovascular
MEDILAS 2
FDA 510(k)
FDA Class 3
·Unknown
MODIFICATION TO PORTABLE INTENSIVE CARE UNIT
FDA 510(k)
FDA Class 3
·Cardiovascular