10,000 results · 506ms · Sources: EU EUDAMED, US FDA

Magnetic Bur Block 8-Hole Plum

FDA UDI
ZIRC DENTAL PRODUCTS, INC.·00840161302236·

E-Z Jett Cassette 5-Place Blue

FDA UDI
ZIRC DENTAL PRODUCTS, INC.·00840161300010·"Holds 5 instruments Open top, rounded holes an...

HELMUT ZEPF

FDA UDI
Helmut Zepf Medizintechnik GmbH·EZPF85194150·TRAY, SURGICAL, INSTRUMENT WASH B...

I.B.S™

FDA UDI
IN2BONES·03760225718223·

Freezpen®

FDA UDI
H & O Equipments SA·15407008484009·

Accurett®

FDA UDI
H & O Equipments SA·15407008486003·

Accurett

FDA UDI
H & O Equipments SA·B386SCO216GBOX1·

Freezpen®

FDA UDI
H & O Equipments SA·15407008484207·

Accurett®

FDA UDI
H & O Equipments SA·15407008486102·

Lifechoice Activox P4L

FDA UDI
Inova Labs, Inc.·08582530040029·The current LifeChoice Activox Portable Oxygen ...

Freezpen

FDA UDI
H & O Equipments SA·B386CLN2O8GBOX1·

Lifechoice Activox P4L

FDA UDI
Inova Labs, Inc.·08582530040043·The current LifeChoice Activox Portable Oxygen ...

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·INGEVITY™ non-MRI Lead Passive Fixation, Preformed Atrial J, INGEVITY™ non-MRI Lead Passive Fixation, Ventricular, INGEV

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·Celsius Thermocool, EZ Steer Thermocool Non-Nav Bi-Directional, Celsius RMT Thermocool, Thermocool SF Bi-directional non

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·THERAPY DUAL 8 CATHETER (NON-IRRIGATED), THERAPY 8MM THERMISTOR ABLATION CATHERER (NON-IRRIGATED) SAFIRE TX CATHETER (NO

Catheter, Percutaneous, Cardiac Ablation, For Treatment Of Atrial Flutter

FDA Pre-Market Approval
FDA Class 3 ·Celsius Thermocool, EZ Steer Thermocool Non-Nav Bi-Directional, Celsius RMT Thermocool, Thermocool SF Bi-directional non

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 3 ·THE BIOMET ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR SYSTEM, THE BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATO

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 3 ·Biomet OrthoPak Non-invasive Bone Growth Stimulator System and Biomet SpinalPak Non-invasive Spine Fusion Stimulator Sys

Stimulator, Bone Growth, Non-Invasive

FDA Pre-Market Approval
FDA Class 3 ·THE BIOMET ORTHOPAK NON-INVASIVE BONE GROWTH STIMULATOR SYSTEM, THE BIOMET SPINALPAK NON-INVASIVE SPINE FUSION STIMULATO

DreamStation 2 System, DreamStation 2 Advanced System

FDA registration
Plexus Electronica S. de R.L. de C.V..·2 products·🇲🇽 Mexico