10,000 results · 145ms · Sources: EU EUDAMED, US FDA

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·CETA DDD MODEL 1230 PACER

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval
FDA Class 3 ·META DDD MODEL 1230 PACER

Implantable Pacemaker Pulse-Generator

FDA Pre-Market Approval
FDA Class 3 ·META DDD MODEL 1230 PACER

FIREBIRD SFS

FDA UDI
Orthofix US LLC·18257200081226·FIREBIRD SPINAL FIXATION SYSTEM, DDD INSTRUMENT...

FIREBIRD SFS

FDA UDI
Orthofix US LLC·18257200081219·FIREBIRD SPINAL FIXATION SYSTEM, DDD INSTRUMENT...

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·CHARITE ARTIFICIAL DISC

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX THREADED FUSION DEVICE

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX TM THREADED FUSION DEVICE

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·PRODISC -L TOTAL DISC REPLACEMENT DEVICE

FDA Pre-Market Approval
VENTAK AV AICD & VENTAK AV II DDD AICD

Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

FDA Pre-Market Approval
FDA Class 2 ·MODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER

Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

FDA Pre-Market Approval
FDA Class 2 ·MODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER

FDA Pre-Market Approval
VENTAK AV DDD FAMILY OF AICD SYSTEMS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·DELTA PACEMAKER SYS; VIGOR DDD MODEL 950

FDA Pre-Market Approval
VENTAK AV DDD FAMILY OF AICD SYSTEMS

Implantable Pulse Generator, Pacemaker (Non-Crt)

FDA Pre-Market Approval
FDA Class 3 ·AUTIMA PACING SYSTEM (META DDD MODEL 1230)

Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

FDA Pre-Market Approval
FDA Class 2 ·MODEL 4553 DUAL CHAM. DDD TEMP.CARDIAC PACEMAKER

Prosthesis, Intervertebral Disc

FDA Pre-Market Approval
FDA Class 3 ·prodisc L Total Disc Replacement

Intervertebral Fusion Device With Bone Graft, Lumbar

FDA Pre-Market Approval
FDA Class 2 ·INTER FIX RP THREADED FUSION DEVICE-REDUCED PROFILE

Generator, Pulse, Pacemaker, External Programmable (For Electrophysiological Studies Only)

FDA Pre-Market Approval
FDA Class 2 ·MICRO-PACE DUAL-CHAMBER, DDD, TEMPORARY CARDIAC PACEMAKER