10,000 results
·
52ms
·
Sources: EU EUDAMED, US FDA
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC GEM MODEL 7227CX, GEM III DR MODEL 7275, GEM III VR MODEL 7231 AND GEM III AT MODEL 7276
Implantable Cardioverter Defibrillator (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·MEDTRONIC. GEM MODEL 7227CX, GEM III DR MODEL 7275, GEM III VR MODEL 7231 AND GEM III AT MODEL 7276
FDA Pre-Market Approval
MEDTRONIC. GEM MODEL 7227CX, GEM III DR MODEL 7275, GEM III VR MODEL 7231 AND GEM III AT MODEL 7276
HUDSON RCI
FDA UDI
TELEFLEX INCORPORATED·04026704594511·Oxygen Catheter
HUDSON RCI
FDA UDI
TELEFLEX INCORPORATED·14026704616425·ADULT Nasal Cannula with 25ft (7.5m) Star Lumen...
HUDSON RCI
FDA UDI
TELEFLEX INCORPORATED·14026704656988·ADULT Nasal Cannula with 25ft (7.5m) Star Lumen...
HUDSON RCI
FDA UDI
TELEFLEX INCORPORATED·04026704594528·Oxygen Catheter
Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled
FDA Pre-Market Approval
FDA Class 3
·MENTOR MEMORY GEL SILICONE GEL-FILLED BREAST IMPLANTS
Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled
FDA Pre-Market Approval
FDA Class 3
·MemoryGel® Ultra High Profile - Extended Range (UH-R) Breast Implants
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·Gel-One
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·Gel-One
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE Alpine Everolimus Eluting Coronary Stent System, XIENCE Sierra Everolimus Eluting Coronary Stent System, XIENCE S
Prosthesis, Breast, Noninflatable, Internal, Silicone Gel-Filled
FDA Pre-Market Approval
FDA Class 3
·NATRELLE SILICONE-FILLED BREAST IMPLANTS
Stent, Iliac
FDA Pre-Market Approval
FDA Class 3
·Omnilink Elite Vascular Balloon-Expandable Stent System
Acid, Hyaluronic, Intraarticular
FDA Pre-Market Approval
FDA Class 3
·Gel-One
CLOST. DIFF. INCL GDH AND/OR TOXIN A AND B - RT & POC
Device
EU IVDD
·
Eu Ivd General
·Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.·On the market·13 countries
Kit, Rna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·Aptima HPV Assay
FDA Pre-Market Approval
GEN-PROBE(R) AMPLIFIED(TM) MYCOBACTERIUM TUBERCULOSIS DIRECT (MTD) TEST
Kit, Rna Detection, Human Papillomavirus
FDA Pre-Market Approval
FDA Class 3
·APTIMA HPV 16 18/45 GENOTYPE ASSAY
Prostrate Cancer Genes Nucleic Acid Amplification Test System
FDA Pre-Market Approval
FDA Class 3
·PROGENSA PCA3 ASSAY