8 results
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34ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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PEDIATRIC SIZED HEMOCATH CATHETER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PRONE STANDER
FDA 510(k)CONTACT LENS CASE FOR SOFT LENSES
FDA 510(k)
FDA Class 2
·Ophthalmic
KANGAROO EPUMP - NEW
FDA Adverse Event
Other
·JABIL SINGAPORE·Product code LZH·May 15, 2014
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM (UNK SIZE)
FDA Adverse Event
Injury
·ALLERGAN·Product code LTI·November 16, 2012
ACRYSOF
FDA Adverse Event
Injury
·ALCON RESEARCH, LTD. / HUNTINGTON·Product code HQL·September 23, 2010
CardioMEMS HF System Hospital and Patient Electronics Units: (a) Patient Electronics System, Model CM1100 (b) Hospital Electronics System, Model CM3000
FDA Recall
Terminated
·Abbott Laboratories, Inc.·Product code MOM·June 14, 2018
CardioMEMS Patient Electronic System (PES), Model Number CM1100. Used for wirelessly measuring and monitoring pulmonary artery pressure and heart rate.
FDA Recall
Open, Classified
·St. Jude Medical·Product code MOM·October 4, 2023