20 results · 50ms · Sources: EU EUDAMED, US FDA

AZUR PURE Peripheral Coil System, Pushable 18

FDA registration
MicroVention Costa Rica S.R.L.·1 product·🇨🇷 Costa Rica

AZUR PURE Peripheral Coil System, Pushable 18

FDA registration
MicroVention, Inc.·1 product·🇺🇸 United States

Synergy Health AST, SRL

FDA registration
Synergy Health AST, SRL·1 product·🇨🇷 Costa Rica

AZUR PURE PERIPHERAL COIL SYSTEM, PUSHABLE 35

FDA registration
Terumo Medical Canada, Inc.·1 product·🇨🇦 Canada

AZUR PURE PERIPHERAL COIL SYSTEM, PUSHABLE 35

FDA 510(k)
FDA Class 2 ·Cardiovascular

Device, Vascular, For Promoting Embolization

FDA classification
FDA Class 2 ·Device, Vascular, For Promoting Embolization

Black Silicone

FDA UDI
COOK INCORPORATED·00827002151468·Black Silicone Filiform DP Ureteral Stent Set W...

INSPIRE 6M"

FDA registration
Steril Verona srl·1 product·🇮🇹 Italy

Cable Assembly, ECG Monitoring

FDA registration
Technical Services for Electronics, Inc.·1 product·🇹🇼 Taiwan

CardioLab v7

FDA registration
GE Medical Systems Information Technologies, Inc.·1 product·🇺🇸 United States

MLCL v6.9.5

FDA registration
PLEXUS CORP.·1 product·🇺🇸 United States

CardioLab v7

FDA registration
GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES·1 product·🇺🇸 United States

INSPIRE 6

FDA registration
SORIN GROUP ITALIA S.R.L·1 product·🇮🇹 Italy

Cook

FDA UDI
COOK INCORPORATED·00827002464407·Black Silicone Filiform Double Pigtail Ureteral...

AGILITY Steerable Guidewire

FDA registration
Cerenovus, Inc.·2 products·🇺🇸 United States

CENTURION MEDICAL PRODUCTS, LP

FDA registration
CENTURION MEDICAL PRODUCTS, LP·2 products·🇺🇸 United States

INSPIRE 6 HOLLOW FIBER OXYGENATOR WITH INTEGRATED HARDSHELL VENOUS/CARDIOTOMY RESERVOIR

FDA 510(k)
FDA Class 2 ·Cardiovascular

CUTERA GENESISPLUS LASER SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis

FDA classification
FDA Class 2 ·Lasers For Temporary Increase Of Clear Nail In Patients With Onychomycosis

Oxygenator, Cardiopulmonary Bypass

FDA classification
FDA Class 2 ·Oxygenator, Cardiopulmonary Bypass