5,924 results · 134ms · Sources: EU EUDAMED, US FDA

Patella Trial <41> mm SFP (264-1-10041)

FDA registration
Straits Orthopaedics (MFG) Sdn Bhd·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

Patella Trial <41> mm SFP (264-1-10041)

FDA registration
STRAITS ORTHOPAEDICS (MFG) SDN BHD·1 product·🇲🇾 Malaysia

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

FDA Pre-Market Approval
FDA Class 3 ·SENSOLOG/DIALOG/REGENCY FAMILY OF PACEMAKERS

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·MEDTRONIC(R) LEGEND PLUS(TM) PULSE GENERATOR

Stent, Carotid

FDA Pre-Market Approval
FDA Class 3 ·Neuroguard IEP® 3-in-1 Carotid Stent, Post-Dilation Balloon System with Integrated Embolic Protection

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·LADARVISION 4000 EXCIMER LASER SYSTEM

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Prospera SCS System Next Generation Active Anchor, TrueLock

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

FDA Pre-Market Approval
FDA Class 3 ·QUADRA ASSURA/UNIFY ASSURA FAMILY OF CRT-DS

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·ELLIPSE/FORTIFY ASSURA FAMILY OF ICDS

Pulse Generator, Permanent, Implantable

FDA Pre-Market Approval
FDA Class 3 ·AFFINITY/INTEGRITY/VICTORY/ZEPHYR/ACCENT FAMILY OF PACEMAKERS

Stimulator, Spinal-Cord, Totally Implanted For Pain Relief

FDA Pre-Market Approval
FDA Class 3 ·Prospera Spinal Cord Stimulation (SCS) System, Resilience Percutaneous Lead, HomeStream Remote Management

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·AFFINITY ANTERIOR CERVICAL CAGE SYSTEM

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

FDA Pre-Market Approval
FDA Class 3 ·MICRONY FAMILY PACEMAKERS

Excimer Laser System

FDA Pre-Market Approval
FDA Class 3 ·ALLEGRETTO WAVE EYE-Q EXCIMER LASER SYSTEM

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

FDA Pre-Market Approval
FDA Class 3 ·FRONTIER/FRONTIER II/ANTHEM FAMILY OF CRT-PS

U2 Total Knee System Tibial Baseplate, CMA, #0

Basic UDI-DI
EU MDD · Eu Md Class 3 ·United Orthopedic Corporation·1 device

U2 Total Knee System Tibial Baseplate, TPS+, #0

Basic UDI-DI
EU MDD · Eu Md Class 3 ·United Orthopedic Corporation·1 device