10,000 results · 45ms · Sources: EU EUDAMED, US FDA

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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