7,410 results · 42ms · Sources: EU EUDAMED, US FDA

METRO-PACIFICA

FDA UDI
Metro Medical Supply·00609626064061·Patient Examination Gloves Powder-Free Vinyl XS

METRO-PACIFICA

FDA UDI
Metro Medical Supply·00609626000137·Patient Examination Gloves Powder-Free Vinyl L

METRO-PACIFICA

FDA UDI
Metro Medical Supply·00609626000076·Patient Examination Gloves Powder-Free Vinyl S

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946430·The DETOUR System is indicated for use for perc...

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946478·The DETOUR System is indicated for use for perc...

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946461·The DETOUR System is indicated for use for perc...

ENDOCROSS Device

FDA UDI
PQ Bypass, Inc.·00860008946409·The DETOUR System is indicated for use for perc...

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946416·The DETOUR System is indicated for use for perc...

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946423·The DETOUR System is indicated for use for perc...

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946447·The DETOUR System is indicated for use for perc...

TORUS Stent Graft System

FDA UDI
PQ Bypass, Inc.·00860008946454·The DETOUR System is indicated for use for perc...

ivWatch Model 400, Device Accessories: Extension Module, SmartTouch Sensor, Patient Cable

FDA 510(k)
FDA Class 2 ·General Hospital

ivWatch® Model 400

FDA 510(k)
FDA Class 2 ·General Hospital

ivWatch

FDA 510(k)
FDA Class 2 ·General Hospital

ivWatch Model 400

FDA 510(k)
FDA Class 2 ·General Hospital

ivWatch Model 400

FDA 510(k)
FDA Class 2 ·General Hospital

NEXUS PAV LUER LOCK DEVICE, MODEL NIS-4

FDA 510(k)
FDA Class 2 ·General Hospital

Lymph Node Location System During Sentinel Biopsy Procedure

FDA Pre-Market Approval
FDA Class 3 ·Magtrace and Sentimag Magnetic Locatization System (PUV)

Sapphire

FDA UDI
ICU MEDICAL FLEET SERVICES, LLC·10887787007432·SAPPHIRE Primary 0.2 Micron Filter Set Non-Vent...

RZ Tunneling Drill

FDA registration
RAZEK EQUIPAMENTOS LTDA·1 product·🇧🇷 Brazil