10 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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IBI-1100 STEERABLE ELECTROPHYSIOLOGY CATHETER SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
De Soutter Medical
FDA UDI
DE SOUTTER MEDICAL LIMITED·05051471149816·K-WIRE - DOUBLE TROCAR FULLY THREADED 1.2mm DIA...
MICRO ANASTOMOSIS CLAMP
FDA 510(k)
FDA Class 2
·Cardiovascular
CORONIS 3MP AND MDCG 3120-CB
FDA 510(k)
FDA Class 2
·Radiology
MENTOR MEMORYGEL BREAST IMPLANT
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·March 22, 2024
EDWARDS SAPIEN XT TRANSCATHETER HEART VLV (23MM)
FDA Adverse Event
Injury
·EDWARDS LIFESCIENCES·Product code NPT·August 3, 2015
MINICAP TRANSFER SET
FDA Adverse Event
Injury
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·February 14, 2013
OT ULTRA2 METER
FDA Adverse Event
Injury
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·July 28, 2014
FLEXOR PARALLEL URETERAL ACCESS SHEATH AND DILATORS
FDA Adverse Event
Injury
·COOK INC·Product code EZN·May 21, 2019
AXIUM PRIME BRPL HLX
FDA Adverse Event
Malfunction
·MEDTRONIC MEXICO·Product code KRD·September 25, 2023