32 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Metacross OTW PTA Balloon Dilatation Catheter
FDA 510(k)
FDA Class 2
·Cardiovascular
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 30, 2022
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·March 18, 2026
METACROSS OTW PTA BALLOON DILATATION CATHETER
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 19, 2019
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·February 7, 2024
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·December 26, 2019
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 12, 2020
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·July 19, 2019
PTA BALLOON CATHETER(OHICHO3)
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·December 13, 2017
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 14, 2020
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 30, 2020
OHICHO NEO
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·July 31, 2025
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·May 28, 2020
OHICHO3
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·September 26, 2018
SHIRANUI EX
FDA Adverse Event
Injury
·KANEKA CORPORATION·Product code LIT·August 7, 2018
OHICHO3
FDA Adverse Event
Injury
·Product code LIT·September 17, 2019
Epredia
FDA UDI
RICHARD-ALLAN SCIENTIFIC COMPANY·00673693063784·The blades and knifes consumables are for use w...
LACTOSORB® 1.5MM SYSTEM
FDA UDI
BIOMET MICROFIXATION, INC·00841036054311·
Staple Sizer - Red
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215165246·
MATRYX INTERFERENCE SCREW
FDA 510(k)
FDA Class 2
·Orthopedic