7,725 results
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39ms
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Sources: EU EUDAMED, US FDA
Terragene Chemdye® (CD16, CD29)
FDA registration
TERRAGENE SA·2 products·🇦🇷 Argentina
Cys-C Rapid Quantitative Test
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Xiamen Biotime Biotechnology Co., Ltd.·1 device
Cystatin C (Cys C) Control
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Maccura Biotechnology Co., Ltd. ·1 device
Cystatin C (Cys C) Control
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Maccura Biotechnology Co., Ltd. ·1 device
Cystatin C (Cys C) Control
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Maccura Biotechnology Co., Ltd. ·1 device
Cystatin C (Cys C) Control
Basic UDI-DI
EU IVDD
·
Eu Ivd General
·Maccura Biotechnology Co., Ltd. ·1 device
JYV CONCEPT
Importer
🇫🇷 France·2 Manufacturers
Doble Access Step
Basic UDI-DI
EU MDR
·
Eu Md Class 1
·JMS- Indústria de Mobiliário Hospitalar, SA·1 device
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE PRIME EVEROLIMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM; XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYS
Block, Cutting, Ent, Non-Sterile
FDA classification
FDA Class 1
·Block, Cutting, Ent, Non-Sterile
Vise, Ossicular Finger, Non-Sterile
FDA classification
FDA Class 1
·Vise, Ossicular Finger, Non-Sterile
Scissors, Wire Cutting, Ent, Non-Sterile
FDA classification
FDA Class 1
·Scissors, Wire Cutting, Ent, Non-Sterile
Stent, Superficial Femoral Artery
FDA Pre-Market Approval
FDA Class 3
·EverFlex Self-Expanding Peripheral Stent System, 2 EverFlex Self-Expanding Peripheral Stent with Entrust Delivery Sys
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·XIENCE PRIME Everolimus Eluting Coronary Stent System / SV / LL ; XIENCE Xpedition Everolimus Eluting Coronary Stent Sys
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·Resolute Onyx Zotarolimus Eluting Coronary Stent System RX and OTW; Onyx Frontier Zotarolimus Eluting Coronary Stent Sys
Coronary Drug-Eluting Stent
FDA Pre-Market Approval
FDA Class 3
·Resolute Onyx Zotarolimus-Eluting Coronary Stent System-RX and OTW, Onyx Frontier Zotarolimus-Eluting Coronary Stent Sys
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·CoreValve EnVeo R Delivery Catheter System, CoreValve EnVeo R Loading System, CoreValve EnVeo Proo Delivery Catheter Sys
Aortic Valve, Prosthesis, Percutaneously Delivered
FDA Pre-Market Approval
FDA Class 3
·CoreValve EnVeo R Delivery Catheter System, CoreValve EnVeo R Loading System, CoreValve EnVeo Pro Delivery Catheter Sys
Stimulator, Bone Growth, Non-Invasive
FDA Pre-Market Approval
FDA Class 3
·Biomet OrthoPak Non-invasive Bone Growth Stimulator System and Biomet SpinalPak Non-invasive Spine Fusion Stimulator Sys
Implant, Cochlear
FDA Pre-Market Approval
FDA Class 3
·FLEX34 Active Electrode, Insertion Electrode (IE) FLEX34, Insertion Probe, Insertion Probe L and Auditory Nerve Test Sys