7 results
·
26ms
·
Sources: EU EUDAMED, US FDA
ACCU-TEC SYSTEM FOR TISSUE EXPANDER INJECTION PORT
FDA 510(k)
FDA Unclassified
·Unknown
CHS
FDA UDI
Smith & Nephew, Inc.·03596010431479·CANNULATED OSTEOTOMY BLADE PLATE ADOLESCENT 3 H...
RET-CHECK
FDA 510(k)
FDA Class 2
·Hematology
LUMATAG(TM) HCG CHEMILUMINESCENCE IMMUNOMETRIC
FDA 510(k)
FDA Class 2
·Clinical Chemistry
CS100 INTRA-AORTIC PUMP
FDA Adverse Event
Malfunction
·DATASCOPE CORP.·Product code DSP·May 28, 2014
ENDOTAK RELIANCE
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVY·January 9, 2013
POWER PRO AMBULANCE COT
FDA Adverse Event
Malfunction
·STRYKER CORP., MEDICAL DIV.·Product code INK·November 12, 2010