8 results
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36ms
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Sources: EU EUDAMED, US FDA
HOTWIRE System RF Generator and Footswitch (optional accessory)
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
Corneal Trephine
FDA UDI
KATENA PRODUCTS, INC.·00841668112687·BARRON CORNEAL PUNCH 9.25MM
ceraMotion®
FDA UDI
DENTAURUM GmbH & Co.KG·J011252083200·ceraMotion® Me Shoulder C, 20 g / dental cerami...
NAVISTAR RMT STEERABLE TIP DIAGNOSTIC CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
Biodegradable Powder Free Nitrile Examination Glove, Blue-White Color with Low Dermatitis Potential Claim and Tested for Use with Chemotherapy Drugs
FDA 510(k)
FDA Class 1
·General Hospital
POINTE SCIENTIFIC, INC. GLUCOSE HEXOKINASE HITACHI REAGENT
FDA Adverse Event
Malfunction
·POINTE SCIENTIFIC, INC.·Product code CFR·December 8, 2008
COATED VICRYL PLUS ANTIBACTERIAL (POLYGLACTIN 910)
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code GAM·September 16, 2011
UNKNOWN ZIMMER MIS TIBIAL COMPONENT
FDA Adverse Event
Injury
·ZIMMER, INC.·Product code JWH·July 25, 2013