8,483 results
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28ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780457046·Integra® Jarit® Handle and Gear for REF#'s 300-...
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780457022·Integra® Jarit® Handle and Gear for REF#'s 300-...
GastroFlex™UHD-C
FDA UDI
MAUNA KEA TECHNOLOGIES·03760187910246·
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780457039·Integra® Jarit® Handle and Gear for REF#'s 300-...
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780457015·Integra® Jarit® Handle and Gear for REF#'s 300-...
Integra® Jarit®
FDA UDI
INTEGRA LIFESCIENCES PRODUCTION CORPORATION·10381780457053·Integra® Jarit® Handle and Gear for REF# 300-26...
GastroFlex™ UHD
FDA UDI
MAUNA KEA TECHNOLOGIES·03760187910079·
ADVISOR¿ HD GRID MAPPING CATHETER, SENSOR ENABLED¿
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DRF·November 29, 2021
ADVISOR¿ HD GRID MAPPING CATHETER, SENSOR ENABLED¿
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DRF·November 29, 2021
ENSITE X EP SYSTEM
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DQK·September 7, 2021
SWARTZ¿ BRAIDED TRANSSEPTAL INTRODUCER, SL0¿, 8.5 F
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code DYB·August 14, 2025
BRAIDED SWARTZ 63CM LAMP45
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL·Product code DYB·April 4, 2023
AGILIS¿ NXT STEERABLE INTRODUCER DUAL-REACH¿ 61 CM SHEATH, MEDIUM CURL, 8.5F
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL·Product code DYB·June 19, 2025
ADVISOR¿ HD GRID MAPPING CATHETER, SENSOR ENABLED¿
FDA Adverse Event
Injury
·ST. JUDE MEDICAL·Product code DRF·December 9, 2022
AF531 EE LEAK 1 4 PT HDG, SU, SINGLE
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code MNS·May 24, 2019
MILTEX LASER COATED SPECULUM
FDA Adverse Event
Malfunction
·MILTEX / INTEGRA·Product code HDG·April 25, 2017
VUMORE SPECULUM
FDA Adverse Event
Injury
·MEDICAL ENGINEERING CO.·Product code HDG·March 19, 1996
ADVISOR¿ HD GRID MAPPING CATHETER, SENSOR ENABLED¿
FDA Adverse Event
Malfunction
·ABBOTT MEDICAL (AFD-PLYMOUTH)·Product code DRF·June 24, 2025
AF531 EE LEAK1
FDA Adverse Event
Injury
·RESPIRONICS, INC.·Product code BZD·August 10, 2023
ADVISOR¿ HD GRID X¿ MAPPING CATHETER, SENSOR ENABLED¿
FDA Adverse Event
Injury
·ABBOTT MEDICAL·Product code MTD·August 21, 2025