10 results
·
27ms
·
Sources: EU EUDAMED, US FDA
DIPRIVAN LUER CONNECTOR
FDA 510(k)
FDA Class 2
·General Hospital
SIC invent Dental Implant Systems
FDA UDI
SIC invent AG·ESIC9352741·SICmax Screw Implant Ø 3.7 mm / 14.5 mm incl. C...
VITALMAX 2100/2200
FDA 510(k)
FDA Class 2
·Cardiovascular
METAL HALIDE LIGHT SOURCE MODEL LM 250
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PERF CON TIB BRG XSML 22X60
FDA Adverse Event
Injury
·BIOMET SPAIN, S.L.·Product code JWH·March 23, 2018
AUTOSOFT XC
FDA Adverse Event
Malfunction
·UNOMEDICAL A/S·Product code FPA·August 9, 2024
HOPKINS TELESCOPE 0°, 5 MM, 29 CM
FDA Adverse Event
Malfunction
·KARL STORZ SE & CO. KG·Product code GCJ·May 16, 2025
9600
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 14, 2013
SM104 M-SERIES W/5TH WHEEL
FDA Adverse Event
Malfunction
·STRYKER CORP, MEDICAL DIVISION·Product code FPO·December 4, 2010
SYSTEM 6 SAGITTAL SAW
FDA Adverse Event
Malfunction
·STRYKER INSTRUMENTS-KALAMAZOO·Product code HWE·July 15, 2014