365 results
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16ms
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Sources: EU EUDAMED, US FDA
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FDA Enforcement
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OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2119.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2115.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2138.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2118.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2117.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2113.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2114.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2111
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2330.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2112
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2110. May be included with the Olympus OER-ELITE.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
OER-ELITE Endoscope Reprocessor Connecting Tubes. Model/Catalog Number: MAJ-2116.
FDA Enforcement
Class II
·Ongoing·Olympus Corporation of the Americas·April 29, 2026
CD4 (SK3), FITC; Contains CD4 FITC with gelatin and 0.1% sodium Azide. Catalog number 340133 in vitro diagnostic used in Hematology: The SK3 monoclonal antibody reacts with human CD4, a 59-kDa cell surface receptor expressed by a majority of thymocytes, a subpopulation of mature T helper cells, and at low levels on monocytes. CD4 is a receptor for the human immunodeficiency virus (HIV).
FDA Enforcement
Class III
·Terminated·Becton, Dickinson and Company, BD Biosciences·September 30, 2015
Carina Ventilator, ventilator. Catalog no. 5704110. Long-term ventilator for treatment in hospitals by a qualified medical personnel.
FDA Enforcement
Class II
·Terminated·Draeger Medical, Inc.·June 6, 2018
GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Part Numbers 00024307507, 00024315007, 00024330007, 00024345007, 00024360007
FDA Enforcement
Class II
·Ongoing·Instrumentation Laboratory·November 29, 2023
Turbett Surgical Container, TS1200: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
FDA Enforcement
Class II
·Ongoing·Turbett Surgical, Inc.·February 8, 2023
Turbett Surgical Container, TS1000: Indicated for enclosing other medical devices that are to be sterilized by a healthcare provider
FDA Enforcement
Class II
·Ongoing·Turbett Surgical, Inc.·February 8, 2023
GEM Premier 3000 PAK - pH, pCO2, pO2, Hct, Na+, K+, Ca++, Glucose and Lactate, Part Numbers 00024315009, 00024330009, 00024345009, 00024360009
FDA Enforcement
Class II
·Ongoing·Instrumentation Laboratory·November 29, 2023
Nellcor SpO2 Upgrade kit, consists of a Nellcor SpO2 circuit board, an OEM part manufactured by a third party supplier; and an integral component of the Nellcor SpO2 device. Controlled infrared heat to neonates who are unable to thermo-regulate based on their own physiology with integrated monitoring feature used for continuous noninvasive monitoring of functional oxygen saturation of arterial hemoglobin (SpO2) and pulse rate (measured by a SpO2 sensor).
FDA Enforcement
Class II
·Terminated·GE Healthcare·May 14, 2014
Precise Digital Accelerator Intended to be used for radiation therapy treatments of malignant neoplastic diseases, as determined by a licensed medical practitioner.
FDA Enforcement
Class II
·Terminated·Elekta, Inc.·February 18, 2015