59 results
·
25ms
·
Sources: EU EUDAMED, US FDA
Filters
Status: Open, Classified
×
IsoLoc Short Profile Prostate Immobilization Treatment Balloon Device Kit; UPN/Catalog Number: ISO-60;
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code PCT·February 4, 2025
VenaCure EVLT KIT WITH SPOTLIGHT OPS SHEATH 55CM Ref./ Catalog No.: EVLT55OPS (each box contains 5 Procedure Kits). For use in the treatment of varicose veins.
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code GEX·August 10, 2022
NanoKnife 5-Probe Procedure Pack 15 cm - Activation. Indicated for the surgical ablation of soft tissue. Catalog Number: 20400111 UPN: H787204001110
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code OAB·March 2, 2023
MINI STICK MAX 5F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-758
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 2.75" PG Catalog Number: 45-756
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 4F X 10CM STIFF .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. - Catalog Number: 45-781
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STIFF .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-759
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-767
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 4F X 10 CM STIFF .018 SS/SS ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-751
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 NI/TU ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-775
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-765
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 4F X 10 CM STIFF .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-752
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 4F X 10 CM STD .018 NI/TU ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-750
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 1.6" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-774
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 4F X 10 CM STD .018 SS/PD ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-749
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 10 CM STD .018 SS/SS ECHO 2.75" PG -Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-754
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 4F X 10 CM STIFF .018 NI/TU NON-ECHO 2.75" PG- Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-762
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
MINI STICK MAX 5F X 15 CM STIFF .018 NI/TU NON-ECHO 2.75" PG-Used for the percutaneous introduction of a guidewire into the vascular system. Catalog Number: 45-776
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DRE·January 30, 2024
SOFT-VU KUMPE 5F X 65CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732701
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DQO·June 18, 2024
SOFT-VU KUMPE 5F X 40CM -Used for patients in need of angiographic diagnosis. Catalog Number: 10732702
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code DQO·June 18, 2024