5,790 results
·
82ms
·
Sources: EU EUDAMED, US FDA
STORQ™ Steerable Guidewire - Standard
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - Soft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - Soft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - Soft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - Soft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - Soft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - Soft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - SuperSoft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
STORQ™ Steerable Guidewire - SuperSoft
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
RAILWAY Sheathless Access System
Device
EU MDR
·
Eu Md Class 2a
·Cordis US Corporation·On the market·32 countries
Device, Hemostasis, Vascular
FDA Pre-Market Approval
FDA Class 3
·EXOSEAL Vascular Closure Device
CORDIS OPTEASE VENA CAVA FILTER, MODELS 466-F220A AND 466-F220B; RETRIEVABLE CATHETER, MODEL 466-C220F
FDA 510(k)
FDA Class 2
·Cardiovascular
PRECISE RX NITINOL STENT TRANSHEPATIC BILIARY SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology