3,088 results · 42ms · Sources: EU EUDAMED, US FDA

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050241533·PAD, TABLE, 1.00 X 27.00 X 78.00

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050243759·PAD, TABLE, 1" x 21" x 42"

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050240888·PAD, TABLE, 1.25" x 26" x 78"

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050244015·PAD, TABLE, 1.5" x 27" x 78"

N/A

FDA UDI
DOMICO MED-DEVICE, LLC·00810050241571·PAD, TABLE, 1.50 X 27.00 X 78.00

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050241526·PAD, TABLE, 1.00 X 24.00 X 72.00

N/A

FDA UDI
DOMICO MED-DEVICE, LLC·00810050241540·PAD, TABLE, 1.00 X 27.00 X 78.00

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050240871·PAD, TABLE, 1" x 24" x 72"

NA

FDA UDI
DOMICO MED-DEVICE, LLC·00810050243766·PAD, TABLE, 1" x 24" x 60"

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Attain Bipolar OTW Lead, Attain OTW L V Lead, Consulta CRT-P, Percepta Bipolar CRT-P, Percepta Quadripolar CR T-P, Seren

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·ACS MULTI-LINK RX/OTW TRISTAR CORONARY STENT SYSTEM

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·EXPRESS/EXPRESS 2 MR & OTW CORONARY STENT SYSTEMS

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·MULTI-LINK RX AND OTW VISION CORONARY STENT SYSTEMS

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·REBEL PLATINUM CHROMIUM CORONARY STENT SYSTEM Monorail & OTW

Catheter, Angioplasty, Peripheral, Transluminal

FDA Pre-Market Approval
FDA Class 2 ·FLEXTOME CUTTING BALLOON MONORAIL(MR)/OVER THE WIRE(OTW)

Coronary Drug-Eluting Stent

FDA Pre-Market Approval
FDA Class 3 ·RESOLUTE INTEGRITY ZOTAROLIMUS-ELUTING CORONARY SYSTEM (RX AND OTW)

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·ACS MULTI-LINK RX/OTW DUET CORONARY STENT SYSTEMS

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·MULTI-LINK ULTRA RX AND OTW CORONARY STENT SYSTEMS

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·MULTI-LINK RX TETRA/OTW TETRA CORONARY STENT SYSTEM

Stent, Coronary

FDA Pre-Market Approval
FDA Class 3 ·S660 2.75 WITH DISCRETE TECHNOLOGY OTW CORONARY STENT SYSTEM