10,000 results · 61ms · Sources: EU EUDAMED, US FDA

Oxy2Pro

FDA UDI
Southmedic Incorporated·10620974003639·Oxy2Pro Procedural Adult Mask with Microstream ...

Oxy2Pro

FDA UDI
Southmedic Incorporated·10620974003622·Oxy2Pro Procedural Adult Mask with Male Luer

Colors in Optics

FDA UDI
Colors In Optics, Ltd.·00781268851541·Readers

Colors in Optics

FDA UDI
Colors In Optics, Ltd.·00781268851510·Readers

Colors in Optics

FDA UDI
Colors In Optics, Ltd.·00781268851503·Readers

Colors in Optics

FDA UDI
Colors In Optics, Ltd.·00781268851527·Readers

Colors in Optics

FDA UDI
Colors In Optics, Ltd.·00781268851497·Readers

Colors in Optics

FDA UDI
Colors In Optics, Ltd.·00781268851534·Readers

SchureMed

FDA UDI
SCHUERCH CORPORATION·00810014601205·Great White Premuim Stirrup--Mizuho Osi Armerica

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MODEL 2920 (PRM) SYSTEM ZOOM (DELTA PACEMAKER SYSTEM)

Pacemaker/Icd/Crt Non-Implanted Components

FDA Pre-Market Approval
FDA Class 3 ·LATITUDE INDUCTIVE COMMUNICATOR ; LATITUDE PROGRAMMER/RECORDER/MONITOR (PRM)

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MODEL 2920 (PRM) SYSTEM ZOOM (VENTAK AV AICD SYSTEM)

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MODEL 2920 PRM SYSTEM ZOOM (VENTAK PRX AICD SYSTEM)

Pulse Generator, Pacemaker, Implantable, With Cardiac Resynchronization (Crt-P)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK RENEWAL TR CRT-P SYSTEM

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·VENTAK MINI AICD SYSTEM

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·DELTA/VISTA AND VIGOR

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CONTAK CD/EASYTRACK CRT SYSTEM

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·VENTAK AV AICD SYSTEM

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·PULSAR/PULSAR MAX/ DISCOVERY/MERIDIAN

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·MODEL 2920 (PRM) SYSTEM ZOOM (VIGOR DR/SR PACEMAKER SYSTEM)