8 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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600 & 900 SERIES ELECTRODES & 755 & 756 HANDLE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
3M™ Forsus™
FDA UDI
3M UNITEK CORPORATION·00652221227973·3M™ Forsus™ Fatigue Resistant Device, 885-200, ...
MODULAR PRESS FIT (MPF) STEM
FDA 510(k)
FDA Class 2
·Orthopedic
EXL-14 MEDICAL LINEAR ACCELERATOR
FDA 510(k)
FDA Class 2
·Radiology
PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·June 19, 2014
CARDINAL
FDA Adverse Event
Malfunction
·CARDINAL HEALTH·Product code OJU·October 21, 2010
ARCHITECT I2000SR ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT MANUFACTURING INC·Product code OMI·December 26, 2012
BIOMET StageOne Select, Hip Stem Cement Spacer Mold w/Reinforcement Cement, 9 X 125 MM, Silicone, Sterile, Item 431190.
FDA Enforcement
Class II
·Terminated·Biomet, Inc.·April 15, 2020