10,000 results
·
45ms
·
Sources: EU EUDAMED, US FDA
My. Size Pro 57
Device
EU MDR
·
Eu Md Class 2b
·Richter Rubber Technology Sdn Bhd·On the market·1 country
My. Size Pro 60
Device
EU MDR
·
Eu Md Class 2b
·Richter Rubber Technology Sdn Bhd·On the market·1 country
My.Size Pro 57
Device
EU MDR
·
Eu Md Class 2b
·Richter Rubber Technology Sdn Bhd·On the market·1 country
My.Size Pro 53
Device
EU MDR
·
Eu Md Class 2b
·Richter Rubber Technology Sdn Bhd·On the market·1 country
My. Size Pro 53
Device
EU MDR
·
Eu Md Class 2b
·Richter Rubber Technology Sdn Bhd·On the market·1 country
My.Size Pro 49
Device
EU MDR
·
Eu Md Class 2b
·Richter Rubber Technology Sdn Bhd·On the market·1 country
PROTECTIVE DEVICES, LUBRICANTS AND SOOTHING DEVICES (SPRAYS, GELS, FLUIDS AND CREAMS)
Device
EU MDD
·
Eu Md Class 2a
·Richter Rubber Technology Sdn Bhd·On the market·2 countries
VARIOUS ULTRASOUND INSTRUMENTS - CONSUMABLES
Device
EU MDD
·
Eu Md Class 2a
·Richter Rubber Technology Sdn Bhd·On the market·2 countries
Defibrillator, Implantable, Dual-Chamber
FDA Pre-Market Approval
FDA Class 3
·LUMAX DR-T, LUMAX VR-T AND LUMAX CRT-D
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Cobalt MRI ICD, Cobalt XT MRI ICD, Crome MRI ICD, Evera MRI DF-1 ICD, Evera MRI ICD, Evera S DR ICD, Evera S VR ICD, Eve
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Consulta CRT-P, Percepta Bipolar CRT-P, Percepta Quadripolar CRT-P, Serena Bipolar CRT-P, Serena Quadripolar CRT-P, Sola
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·Advisa DR IPG, Advisa DR MRI IPG, Advisa SR MRI IPG, Astra S DR MRI IPG, Astra S SR MRI IPG, Astra XT DR MRI IPG, Astra
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·Amplia MRI CRT-D, Amplia MRI Quad CRT-D, Brava CRT-D, Brava Quad CRT-D, Claria MRI CRT-D, Claria MRI Quad CRT-D, Cobalt
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·Aurora EV ICD
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·IDENTIFY, VERITY, VICTORY, ZEPHYR, ACCENT FAMILY OF PACEMAKER DEVICES
Pulse Generator, Permanent, Implantable
FDA Pre-Market Approval
FDA Class 3
·ATLAS/ATLAS+, ATLAS II/ATLAS II+, CURRENT, CURRENT ACCEL, CURRENT+, EPIC/EPIC+, EPIC II/EPIC II+, FORTIFY
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·ATLAS+ HF/ATLAS II HF, ATLAS II+ HF, EPIC+, EPIC II HF, EPIC II+HF, PROMOTE, PROMOTE+, PROMOTE, RF, PROMOTE ACCEL, UNIFY
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·FRONTIER, FRONTIER II, ANTHEM FAMILY OF CRT-P DEVICES
Slip-Cath
FDA UDI
COOK INCORPORATED·00827002120464·Slip-Cath, Infusion Catheter
Slip-Cath
FDA UDI
COOK INCORPORATED·00827002120426·Slip-Cath, Infusion Catheter