7 results
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19ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BIVONA CUFF MAINTENANCE DEVICE (CMD)
FDA 510(k)
FDA Class 2
·Anesthesiology
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450806524·
SITE PHACOEMULSIFICATION HANDPIECE
FDA 510(k)
FDA Class 2
·Ophthalmic
AFB (ABSORBABLE FOAM BUTTRESS)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
DUR MAR +4 10D LNR 36X60
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·January 14, 2013
ASR ACETABULAR CUPS 56
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL, LTD.·Product code KWA·December 1, 2010
SOFTCLIX ® PLUS LANCET DEVICE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code FMK·July 3, 2014