8 results
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29ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ALWAYS MENSTRUAL PADS
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
PARADIGM SOF-SET MICRO QR, MODELS 324 AND 325
FDA 510(k)
FDA Class 2
·General Hospital
ORTELIUS 800
FDA 510(k)
FDA Class 1
·Orthopedic
SPECTRA WAVEWRITER?
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·December 19, 2025
SYRINGE 3ML LL W/NDL 25X5/8 RB
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 19, 2019
CAPSUREFIX NOVUS
FDA Adverse Event
Injury
·MPRI·Product code DTB·April 22, 2013
SYMBIQ 3.13 SINGLE C
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·August 12, 2014
DAILY ACTIVITY ASSIST DEVICES- UTENSIL FOR DRESSING, GROOMING, RECREAT
FDA Adverse Event
Injury
·UNK·Product code INM·April 23, 2011