239 results
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26ms
·
Sources: EU EUDAMED, US FDA
THAYER-MARTIN, MODIFIED
FDA 510(k)
FDA Class 2
·Microbiology
EasyTouch
FDA UDI
MHC MEDICAL PRODUCTS, LLC·MHC18300612·EasyTouch 30G Pressure Activated Safety Lancet
iNSitu™ Hip System
FDA UDI
NEXTSTEP ARTHROPEDIX, LLC·00816127023613·Full Hemisphere Reamer Size 61
Persona®
FDA UDI
Zimmer, Inc.·00889024559714·
Persona®
FDA UDI
Zimmer, Inc.·00889024559530·
Persona®
FDA UDI
Zimmer, Inc.·00889024559448·
Persona®
FDA UDI
Zimmer, Inc.·00889024559622·
PS 3000 DIGATAL PHOTOSPOT SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
PICCOLO COMPOSITE PLATE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
SYNCHROMED II
FDA Adverse Event
Injury
·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 13, 2012
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 23, 2014
SECURE 3 MED/SURG BED
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV.·Product code FNL·September 7, 2010
CERTAIN® LOW PROFILE ONE-PIECE ABUTMENT 4.1MM(D) X 2MM(H)
FDA Adverse Event
Malfunction
·BIOMET 3I·Product code NHA·May 31, 2018
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·STEROID TIP(TM) MODEL 4503&4003 TRANSVENOUS PACING
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE SENSE LEAD
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE SENSE LEAD, CAPSURE SP NOVUS LEAD, VITATRON CRYSTALLINE LEAD; VITATRON EXCELLENCE LEAD PS+LEAD
Drug Eluting Permanent Right Ventricular (Rv) Or Right Atrial (Ra) Pacemaker Electrodes
FDA Pre-Market Approval
FDA Class 3
·CapSure Sense Lead, Vitatron Crystalline Lead
Permanent Pacemaker Electrode
FDA Pre-Market Approval
FDA Class 3
·CAPSURE FAMILY OF LEADS/ACCESSORIES
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE SENSE BIPOLAR LEAD
Permanent Defibrillator Electrodes
FDA Pre-Market Approval
FDA Class 3
·CAPSURE, VITATRON CRYSTALINE AND VITATRON EXCELLENCE PS