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