29 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Monitor,Test,Hiv-1
FDA classification
FDA Class 3
·Monitor,Test,Hiv-1
Implant, Dermal, For Aesthetic Use
FDA Pre-Market Approval
FDA Class 3
·RESTYLANE/PERLANE/RESTYLANE-L/PERLANE-L INJECTABLE GELS
Tissue Graft Of 6mm And Greater
FDA Pre-Market Approval
FDA Class 3
·ProCol Vascular Bioprosthesis
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEL 80 Excimer Laser
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEL 80 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEL 80 Excimer Laser System
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEL 80 Excimer Laser System
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEL 80 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEL 90 EXCIMER LASER SYSTEM
Excimer Laser System
FDA Pre-Market Approval
FDA Class 3
·MEDITEC MEL 80 EXCIMER LASER SYSTEM
Lenses, Soft Contact, Extended Wear
FDA Pre-Market Approval
FDA Class 3
·CSI (CROFILCON A) EXTENDED WEAR SOFT
Kit, Test, In Vitro Periodontal
FDA Pre-Market Approval
FDA Class 3
·PERIOCHECK TM ENZYME ACTIVITY TEST KIT
Kit, Test, In Vitro Periodontal
FDA Pre-Market Approval
FDA Class 3
·PERIOCHECK TM ENZYME ACTIVITY TEST KIT
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC(R) MDL 6966, 6936, 6963 TRANSVENE(R) AND MODEL 6939 AND 6999 SUBCUTANEOUS PATCH LEADS.
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·CADET V-105 C AND D AND V-115 C AND D PULSE GENERATORS & SOFTWARE VERSION 4.1 FOR THE PROGRAMMER MDL PR-1500
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·COFLEX® INTERLAMINAR TECHNOLOGY
Prosthesis, Spinous Process Spacer/Plate
FDA Pre-Market Approval
FDA Class 3
·coflex Interlaminar Stabilization Device