2,705 results · 26ms · Sources: EU EUDAMED, 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