72 results
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21ms
·
Sources: EU EUDAMED, US FDA
Implantable Pulse Generator, Pacemaker (Non-Crt)
FDA Pre-Market Approval
FDA Class 3
·DDD PULSE GENERATOR 674
Rutter Stent
FDA UDI
Boston Medical Products, Inc.·14063107101721·Size: 14 mm; Type: Radiopaque
Rutter Stent
FDA UDI
Boston Medical Products, Inc.·EBES8400140·Size: 14 mm; Type: Radiopaque
n/a
FDA UDI
Hager & Meisinger Gesellschaft mit beschränkter Haftung·E0HM51008403140141·Rotary diamond instrument for dental application
NAR
FDA UDI
NORTH AMERICAN RESCUE, LLC·20842209122404·
NTI
FDA UDI
NTI - Kahla GmbH Rotary Dental Instruments·E310840014MFG1·NTI Diamond Medium FG
Plateau-X Spacer System
FDA UDI
Life Spine, Inc.·00190837017484·
NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM
FDA Adverse Event
Malfunction
·COCHLEAR LTD.·Product code MCM·August 23, 2016
Panama™
FDA UDI
FLOSPINE LLC·B1830808400140·Self Tapping Bicortical Fixed Screw, 4.0x14mm
NA
FDA UDI
Zimmer, Inc.·00889024101777·
NA
FDA UDI
Zimmer, Inc.·00889024101784·
CHEMODENT CERAMIC METAL
FDA 510(k)
FDA Class 2
·Dental
NUCLEUS 22
FDA Adverse Event
Injury
·COCHLEAR LIMITED·Product code MCM·May 18, 2025
NA
FDA UDI
Zimmer, Inc.·00889024073821·
NA
FDA UDI
Zimmer, Inc.·00889024073814·
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·IBI THERAPY CARDIAC ABLATION SYSTEM ERS/ 1500T RF GENERATOR
Cardiac Ablation Percutaneous Catheter
FDA Pre-Market Approval
FDA Class 3
·MAGiC Ablation Catheter
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 29, 2014
MEDTRONIC INFUSE BONE GRAFT OR RHBMP2
FDA Adverse Event
Injury
·MEDTORNIC, INC.·Product code NEK·November 15, 2012
INNERVISION SNAP SHUNT VENT CATH, BG, 5CM
FDA Adverse Event
Injury
·MEDTRONIC NEUROSURGERY·Product code JXG·September 10, 2010