105 results
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18ms
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Sources: EU EUDAMED, US FDA
Filters
Classification: FDA Class 3
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Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·Cannula with Guide
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc C: prodisc C SK, prodisc C Nova, prodisc C Vivo
Surgical Cardiac Ablation Device, For Treatment Of Atrial Fibrillation
FDA Pre-Market Approval
FDA Class 3
·EPi-Sense ST RF Cable
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc C
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM
Prosthesis, Intervertebral Disc
FDA Pre-Market Approval
FDA Class 3
·prodisc C, prodisc C Vivo, prodisc C Nova, prodisc C SK
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT(TM) CK SYSTEM
Electrosurgical, Radio Frequency, Refractive Correction
FDA Pre-Market Approval
FDA Class 3
·VIEWPOINT CK SYSTEM (KERATOPLAST TIP COMPONENT)
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune Gio
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune System
Stimulator, Low Electric Field, Tumor Treatment
FDA Pre-Market Approval
FDA Class 3
·Optune®
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens (LAL), Light Delivery Device (LDD) System
Endovascular System For Treatment Of Thoracoabdominal And Pararenal Aortic Lesions
FDA Pre-Market Approval
FDA Class 3
·GORE® EXCLUDER® Thoracoabdominal Branch Endoprosthesis
Light Adjustable Lens (Lal) And Light Delivery Device (Ldd)
FDA Pre-Market Approval
FDA Class 3
·Light Adjustable Lens, Light Delivery Device