4,642 results
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42ms
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Sources: EU EUDAMED, US FDA
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·SYNERGYST II MEDTRONIC MODEL 9889E SOFTWARE
Raz
FDA UDI
Raz Design Inc·00628758002000·Individually configured, mobile and stationary ...
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Sensar 1-piece IOL, Tecnis 1-piece IOL, Tecnis 1-piece Optiblue IOL, Preloaded Tecnis 1-piece IOL, Preloaded Tecnis 1-pi
Intraocular Lens
FDA Pre-Market Approval
FDA Class 3
·Sensar 1-Piece IOL, Tecnis 1-Piece IOL, Tecnis 1-Piece OptiBlue IOL, Preloaded Tecnis 1-Piece IOL, Preloaded Tecnis 1-Pi
Allergen Discs Bienengift (Apis mellifera)
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Gold Standard Diagnostics Kassel GmbH·1 device
Cranial 4Pi Wedges and Spacers
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·Brainlab AG·4 devices
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·DEMA/DIVA IMPLANTABLE PULSE GENERATORS
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·GEM & MARQUIS FAMILY ICD'S
Pulse-Generator, Single Chamber, Sensor Driven, Implantable
FDA Pre-Market Approval
FDA Class 3
·ACTIVITRAX PACEMAKER FAMILY
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC JEWEL/GEM ICD'S
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC/VITATRON CARELINK PROGRAMMER
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC INSYNC (TM) BIVENTRICAL PACING SYSTEM
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·KAPPA 400 PACEMAKER FAMILY
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC GEM ICD
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·LEGEND PLUS PACEMAKER FAMILY
Implantable Pacemaker Pulse-Generator
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC KAPPA/SIGMA PACEMAKER FAMILIES
Allergen Discs Api m1 Phospholipase A2
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Gold Standard Diagnostics Kassel GmbH·1 device
Pain Therapy Device(Model: DH-P.T.S-I, DH-P.T.S-II, DH-P.T.S-IIA, DH-P.T.S-IIB, DH-CP-I)
FDA 510(k)
FDA Class 2
·Physical Medicine
CSM-BC400-L
FDA registration
RONDISH COMPANY LIMITED·1 product·🇭🇰 Hong Kong
QUIES SAS
Importer
🇫🇷 France