10,000 results
·
54ms
·
Sources: EU EUDAMED, US FDA
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·MICRO STENT TM II, MICRO STENT TM II XL, GFX TM, GFX TM XL
630.00 scissors gfx curved 13cm
Device
EU MDR
·
Eu Md Class 1
·Prodont-Holliger·On the market
WVSM Pro (Series) (500-0030-XX)
FDA 510(k)
FDA Class 2
·Cardiovascular
Epredia PrintMate Slotted Cassette
FDA registration
FA-Tech Diagnostics Europe BV·1 product·🇳🇱 Netherlands
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX-XP/GFX2 CORONARY STENT SYSTEM
VDRIVE W/V-SONO
FDA registration
I-Tek Medical, Inc.·2 products·🇺🇸 United States
Magellan Robotic Catheter 9Fr (50cm, 65cm, 80cm)
FDA registration
Sterigenics U.S. LLC·2 products·🇺🇸 United States
Magellan Robotic Catheter 9Fr (50cm, 65cm, 80cm)
FDA registration
Sterigenics US LLC·2 products·🇺🇸 United States
Steerable Catheter (short, mediu, long) Magellan NorthStar Robotic Catheter
FDA registration
Sterigenics US LLC·2 products·🇺🇸 United States
STEREOTAXIS, INC.
FDA registration
STEREOTAXIS, INC.·2 products·🇺🇸 United States
STEREOTAXIS, INC.
FDA registration
STEREOTAXIS, INC.·2 products·🇺🇸 United States
VDRIVE WITH V-LOOP
FDA registration
I-Tek Medical, Inc.·2 products·🇺🇸 United States
DDU-1XX Series Pediatric Pads Configuration
FDA UDI
DEFIBTECH, L.L.C.·10815098020437·
DDU-1XX Series Battery Pack Configuration
FDA UDI
DEFIBTECH, L.L.C.·10815098020376·
DDU-1XX Series Adult Rescue Pads
FDA UDI
DEFIBTECH, L.L.C.·00815098020423·
DDU-1XX series Battery Pack Configuration
FDA UDI
DEFIBTECH, L.L.C.·10815098020369·
408.05SI scaler double gfx 21 xl
Device
EU MDR
·
Eu Md Class 1
·Prodont-Holliger·On the market
406.05SI scaler double gfx 1 xl
Device
EU MDR
·
Eu Md Class 1
·Prodont-Holliger·On the market
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX OVER-THE-WIRE CORONARY STENT SYSTEM
Stent, Coronary
FDA Pre-Market Approval
FDA Class 3
·GFX 2 OVER-THE-WIRE CORONARY STSENT SYSTEM