6 results
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24ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Prime E-CLASS XLPE Liner
FDA 510(k)
FDA Class 2
·Orthopedic
SUTURE LOCK NAIL BONE ANCHOR WITH WHITE (KFX-W-200) & BLUE (KFX-B-200) FIBERFORCE SUTURE
FDA 510(k)
FDA Class 2
·Orthopedic
EMM SURGICAL DRAPE SMS W/PE SIDES MODEL 13-005 (WITH MINOR DIMENSIONAL VARIATIONS FOR ALTERNATE CONFIGURATIONS)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·June 21, 2013
ENDEAVOR SPRINT RX CORONARY STENT SYSTEM
FDA Adverse Event
Malfunction
·MEDTRONIC IRELAND·Product code NIQ·July 6, 2011
ZYMED HOLTER SOFTWARE
FDA Adverse Event
Injury
·PHILIPS MEDICAL SYSTEMS·Product code DPS·September 26, 2008