7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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UFI GEL HARD
FDA 510(k)
FDA Class 2
·Dental
TSRH SPINAL SYSTEM
FDA Adverse Event
Injury
·WARSAW ORTHOPEDIC, INC·Product code KWP·December 18, 2014
PEAK FLOW RATE METER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
MODEL 7700A/77010A/77025A/77030A/77035A ULTRA IMAG
FDA 510(k)
FDA Class 2
·Cardiovascular
AVAULTA SOLO POSTERIOR SYNTHETIC SUPPORT SYSTEM
FDA Adverse Event
Injury
·BARD SHANNON LIMITED·Product code OTP·March 4, 2013
MESHGRAFT II DERMATOME WITH RATCHET
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL·Product code GFD·January 13, 2011
CAPSUREFIX MRI SURESCAN
FDA Adverse Event
Malfunction
·MPRI·Product code NVN·August 8, 2014