7 results
·
18ms
·
Sources: EU EUDAMED, US FDA
GENERAL PROCEDURAL STRETCHERS (P880- P886)
FDA 510(k)
FDA Class 2
·General Hospital
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471150607·K-WIRE - DOUBLE TROCAR 2.0mm DIA x 230mm
EZ SPLINT & EZ SPLINT PM
FDA 510(k)
FDA Unclassified
·Unknown
Advin Multi-Drug Screen Test Cassette, Dip Card and Cup
FDA 510(k)
FDA Class 2
·Clinical Toxicology
NOVASURE ABLATION KIT
FDA Adverse Event
Malfunction
·HOLOGIC, INC.·Product code MNB·June 19, 2014
XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA·Product code NIQ·December 13, 2010
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·January 18, 2013