56 results
·
27ms
·
Sources: EU EUDAMED, US FDA
CARESIDE LYTES, CARESIDE ANALLYZER MODEL 1000
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ReLine
FDA UDI
Nuvasive, Inc.·00195377080516·RELINE C Drill Guide, 12mm Static
Dukal
FDA UDI
Dukal LLC·10665973000036·Laparotomy Sponges 8" x 36", Sterile
MSI
FDA UDI
Modern Surgical Instruments LLC·00810130207374·XL CERVICAL MICRO CURETTE FORWARD ANGLE #00
Intravascular Radiation Delivery System
FDA Pre-Market Approval
FDA Class 3
·CORDIS CHECKMATE(TM) SYSTEM
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575407538·Orthopaedic implant inserter/extractor, reusabl...
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575407576·Orthopaedic bone nut - Endo Model Knee System
Patriot Spinal Fixation System
FDA UDI
VALORUS SPINE LLC·00811771032912·Rod Pusher
Endo-Model Knee System - Instruments
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575407521·Orthopaedic prosthesis instrument, reusable - G...
LINK Instruments - Wrenches
FDA UDI
WALDEMAR LINK GmbH & Co. KG·04026575407859·Orthopaedic prosthesis instrument, reusable - G...
NEXGEN FEMORAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·April 2, 2024
DIGITAL BPM
FDA 510(k)
FDA Class 2
·Cardiovascular
SYSTEM 1.5 STERILE PROCESSING SYSTEM
FDA 510(k)
FDA Class 2
·General Hospital
NEXGEN COMPLETE KNEE SOLUTION ROTATING HINGE KNEE TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·December 10, 2018
ROTATING HINGE KNEE FEMORAL
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·December 10, 2018
ARTICULAR SURFACE FEM
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code KRO·December 10, 2018
NEXGEN CEMENTED STEM EXT
FDA Adverse Event
Injury
·ZIMMER BIOMET, INC.·Product code JWH·December 10, 2018
Intravascular Radiation Delivery System
FDA Pre-Market Approval
FDA Class 3
·CORDIS CHECKMATE SYSTEM
Intravascular Radiation Delivery System
FDA Pre-Market Approval
FDA Class 3
·CORDIS CHECKMATE SYSTEM
Intravascular Radiation Delivery System
FDA Pre-Market Approval
FDA Class 3
·CORDIS CHECKMATE(TM) SYSTEM