8,495 results
·
51ms
·
Sources: EU EUDAMED, US FDA
NMT Monitoring Cable EMG (3.5m)
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Xavant Technology (Pty) Ltd·1 device
STIMPOD
Basic UDI-DI
EU MDR
·
Eu Md Class 2a
·Xavant Technology (Pty) Ltd·8 devices
Avance Flex Negative Pressure Wound Therapy Canister, 300ML
FDA UDI
APRIA HEALTHCARE LLC·00860385000824·300ml Avance Flex Canister for use with the Ava...
Avance Flex 2.0 Negative Pressure Wound Therapy Pump
FDA UDI
APRIA HEALTHCARE LLC·00860385000855·Avance Flex Pump
Catheters, Transluminal Coronary Angioplasty, Percutaneous
FDA Pre-Market Approval
FDA Class 2
·NC MONORAIL PTC CATHETER, QUANTUM MONORAIL PTCA CATHETER, MAXXUM PTCA CATHETER, VIVA PTCA CATHETER AND ADANTE PTCA CATHR
Avanos Medical Belgium BV
Authorized representative
🇧🇪 Belgium·1 Manufacturer
ADVANT INT ADV PCB 5R MESA B
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·INDUSTRIAS HIDRÁULICAS PARDO SL·86 devices
Avanti Germany
Authorized representative
🇩🇪 Germany·1 Manufacturer·2 Devices
ES19/86843
Certificate
MDD Annex II (excluding section 4)·Xavant Technology (Pty) Ltd·SGS Belgium NV·3 Basic UDI-DIs
TECNOLOGIE AVANZATE TA SRL
Importer
🇮🇹 Italy
Avanos Medical Belgium BV
Importer
🇧🇪 Belgium
TECNOHEALTH SRL
Importer
🇮🇹 Italy·1 Manufacturer
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·IDENTITY XL DR MODEL 5376 PULSE GENERATOR
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·IDENTITY SR MODEL 5172 PULSE GENERATOR
Programmer, Pacemaker
FDA Pre-Market Approval
FDA Class 3
·IDENTITY PULSE GENERATOR MODEL DR 5370
Pulse-Generator, Single Chamber, Sensor Driven, Implantable
FDA Pre-Market Approval
FDA Class 3
·MICRONY PACEMAKERS
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK PRX AND MINI IMPLANTABLE CARDIOVERTER DEFIBRILLATORS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·VENTAK AV, PRIZM, VITALITY, VITALITY AVT IMPLANTABLE CARDIOVERTER DEFIBRILLATORS
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·IDENTITY ADX MODELS XL DR 5386 AND DR 5380 PULSE GENERATORS AND PROGRAMMER SOFTWARE MODEL 3307 V4.2A
Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)
FDA Pre-Market Approval
FDA Class 3
·CONTAK CD AND RENEWAL CARDIAC RESYNCHRONIZATION THERAPY DEFIBRILLATORS