7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
NTI CLENCHING SUPPRESSION SYSTEM
FDA 510(k)
FDA Unclassified
·Unknown
Polystar Selection EDITION
FDA UDI
Merz Dental GmbH·D7091981546·anteriors; shade A2 light; mould BM2
SMALL BONE LOCKING PLATING SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
Dillard Nasal Balloon Catheter
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
P.F.C.* FLUT TIB ROD 115X16MM
FDA Adverse Event
Injury
·DEPUY IRELAND·Product code JWH·February 27, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·August 5, 2014
STENOSCOP
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS (INDIA) PRIVIATE LTD.·Product code JAA·January 31, 2011