4 results
·
24ms
·
Sources: EU EUDAMED, US FDA
RADIESSE
FDA Adverse Event
*·Product code LMH·February 2, 2005
PENUMA IMPLANT
FDA Adverse Event
Injury
·INTERNATIONAL MEDICAL DEVICES, INC.·Product code MIB·October 7, 2019
LEAD ADAPTER, 21 CFR 870.3620
FDA Adverse Event
Injury
·GREATBATCH MEDICAL·Product code DTB·April 1, 2015
PUMP MMT-1780KPK 670G PATHWAY BLACK MG
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OZP·June 28, 2019