9,794 results · 37ms · Sources: EU EUDAMED, US FDA

1001005 / 260-801-001

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Spreader

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

1001110 / IRC

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

STOMA-Cannula

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Needles

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Wax instrument

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Measuring Caliper, Ruler, Caliper

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Curette

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Bone rongeur forceps

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Cutting Instrument

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Wire forceps, Rubber ring removing forceps, Flat pliers, Round pliers, Pin bending pliers, Wire bending pliers

FDA registration
STORZ AM MARK GMBH·1 product·🇩🇪 Germany

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·ADVANTIO, INGENIO, VITALIO, FORMIO, ESSENTIO, ACCOLADE, PROPONENT, INSIGNIA, ALTRUA 2

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

FDA Pre-Market Approval
FDA Class 3 ·INVIVE, INTUA, VISIONIST, VALITUDE

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval
FDA Class 3 ·COGNIS, ENERGEN, PUNCTUA, INCEPTA, ORIGEN, INOGEN, DYNAGEN, AUTOGEN, RESONATE, MOMENTUM, VIGILIANT

Defibrillator, Automatic Implantable Cardioverter, With Cardiac Resynchronization (Crt-D)

FDA Pre-Market Approval
FDA Class 3 ·CRT-D Resynchronization Devices COGNIS, ENERGEN, PUNCTUA, INCEPTA, ORIGEN, INOGEN, DYNAGEN, AUTOGEN, RESONATE, MOMENTUM,

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·EMBLEM S-ICD

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·LATITUDE Wave Communicator

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Pacemaker Devices: ADVANTIO, INGENIO, VITALIO, FORMIO, ESSENTIO, ACCOLADE, PROPONENT, (INSIGNIA and ALTRUA II supported

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Pacemaker Devices: INGENIO MRI, VITALIO MRI, FORMIO MRI, ESSENTIO MRI, PROPONENT MRI, ACCOLADE MRI

Implantable Cardioverter Defibrillator (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·Subcutaneous ICD Devices: EMBLEM