3,540 results · 46ms · Sources: EU EUDAMED, US FDA

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·Cobra PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·COBRA PzF NanoCoated Coronary Stent System

Malaria P.f./Pan Antigen Rapid Test Device

Device
EU IVDD · Eu Ivd General ·Hangzhou Realy Tech Co.,Ltd.·On the market

Malaria P.f. Rapid Test Device (whole blood)

Device
EU IVDD · Eu Ivd General ·Hangzhou Cybereagen Biotech Co., Ltd.·On the market

Malaria P.f &P.v Rapid Test (Whole Blood)

Device
EU IVDD · Eu Ivd General ·Sejoy Biomedical Co., Ltd.·On the market

Malaria P.f &Pan Rapid Test (whole blood)

Device
EU IVDD · Eu Ivd General ·Sejoy Biomedical Co., Ltd.·On the market

PHOENIX 5 URODYNAMICS SYSTEM

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

EVIS EXERA COLONOVIDEOSCOPE CF-Q160 AL/I AND PCF-160 AL/I

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

20 ML NORMAL SALINE TOPICAL SOLUTION, 0.9% W/V SODIUM CHLORIDE

FDA 510(k)
FDA Unclassified ·Unknown