2,705 results
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26ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Intraoral X-ray sensor
FDA UDI
REMEDI CO.,LTD.·08800060100052·
Intraoral X-ray sensor
FDA UDI
REMEDI CO.,LTD.·08800060100069·
IODINE 200 UG/L
FDA UDI
UTAK LABORATORIES, INC.·B800IOD200PM0·IODINE 200 UG/L
IODINE 20 UG/L
FDA UDI
UTAK LABORATORIES, INC.·B800IOD20PM0·IODINE 20 UG/L
STAAR ICL CALCULATION SOFTWARE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·May 20, 2026
STAAR ICL CALCULATION SOFTWARE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·May 21, 2026
CURLIN PAINSMART IOD
FDA Adverse Event
MOOG MEDICAL DEVICES GROUP·Product code FRN·March 11, 2016
STAAR ICL CALCULATION SOFTWARE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·May 19, 2026
CURLIN PAINSMART IOD
FDA Adverse Event
MOOG MEDICAL DEVICES GROUP·Product code FRN·March 11, 2016
IODINE 200 UG/L
FDA UDI
UTAK LABORATORIES, INC.·B800IOD200V2ADX0·IODINE 200 UG/L
IODINE 20 UG/L
FDA UDI
UTAK LABORATORIES, INC.·B800IOD20V2ADX0·IODINE 20 UG/L
STAAR ICL CALCULATION SOFTWARE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·April 30, 2026
STAAR ICL CALCULATION SOFTWARE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·April 30, 2026
STAAR ICL CALCULATION SOFTWARE
FDA Adverse Event
Malfunction
·STAAR SURGICAL COMPANY·Product code MTA·April 30, 2026
DA VINCI SURGICAL SYSTEM
FDA Adverse Event
Other
·INTUITIVE SURGICAL, INC.·Product code KOG·July 21, 2006
20/30 PRIORITY PACK W/COPILOT
FDA Adverse Event
Injury
·GUIDANT VASCULAR INTERVENTION·Product code DTL·December 14, 2001
CURLIN INFUSION PAINSMART IOD IV PUMP
FDA Adverse Event
Malfunction
·MOOG MED DEVICES GROUP·Product code FRN·September 1, 2011
CURLIN INFUSION PAINSMART IOD IV PUMP
FDA Adverse Event
Malfunction
·MOOG MED DEVICES GROUP·Product code FRN·September 1, 2011
CURLIN INFUSION PAINSMART IOD IV PUMP
FDA Adverse Event
Malfunction
·MOOG MEDICAL DEVICES GROUP·Product code FRN·September 7, 2011
CURLIN INFUSION PAINSMART IOD IV PUMP
FDA Adverse Event
Malfunction
·MOOG MED DEVICES GROUP·Product code FRN·September 1, 2011