9 results
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18ms
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Sources: EU EUDAMED, US FDA
IsoLoc Prostate Immobilization Treatment Balloon Device Kit, Catalog/UPN: ISO-100
FDA Recall
Open, Classified
·Angiodynamics, Inc.·Product code PCT·May 21, 2024
Glass Body For 194 Ellik Evacuator. Model Number: 190A. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code KQT·June 18, 2025
Pruitt Irrigation Occlusion Catheter. Catalog Numbers: 2102-09, E2102-09.
FDA Recall
Open, Classified
·LeMaitre Vascular, Inc.·Product code DQT·April 11, 2025
Ellik Latex Bulb, Ellik Evacuator. Model Number: 194-2. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code KQT·June 18, 2025
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
Ellik Evacuator. Model Number: 194. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code KQT·June 18, 2025
Cone with Male Tubing, Non-Locking, Ellik Evacuator. Model Number: 191-NRS. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code KQT·June 18, 2025
Tubing for Male Connector 194, Ellik Evacuator. Model Number: 190-4. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code KQT·June 18, 2025
Ellik Evacuator Adapter, Locking. Model Number: 190-NRS. The Ellik Evacuator and adapter accessories are compatible with Gyrus ACMI Elite and Elite 2 Resection Sheaths.
FDA Recall
Open, Classified
·Olympus Corporation of the Americas·Product code KQT·June 18, 2025