7 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IMWXDOP IR
FDA 510(k)
FDA Class 2
·Radiology
WET SKIN SCRUB TRAY STERILE WET SKIN SCRUB KIT
FDA 510(k)
FDA Class 1
·General Hospital
MICRO-MIST NEBULIZER
FDA 510(k)
FDA Class 2
·Anesthesiology
ALARIS SE ADMINISTRATION SET
FDA Adverse Event
Malfunction
·CAREFUSION CORPORATION·Product code FPA·May 7, 2014
ENDO STICTH POLYSORB 0 48 VIO DLU SU
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US·Product code KOG·January 9, 2013
PLUM A+ DRIVER NEW 8
FDA Adverse Event
Malfunction
·HOSPIRA, INC.·Product code FRN·December 6, 2010
PKG, 5MM INSERT, RIGHT ANGLE FORCEP, 45CM P/N 0250080729 Laparoscopic Manual Instruments are intended for cutting, holding, grasping and manipulating of tissue, organs, organ areas and surgical auxiliaries such as suturing material. Some instruments have radio frequency (RF) ports which allow them to be used for electrosurgery. Laparoscopic surgical manual instruments are designed to be used endoscopically through cannulae to perform cutting, grasping, dissecting, retracting, and manipulating functions. This device does not sustain or support life.
FDA Enforcement
Class II
·Terminated·Stryker Endoscopy·December 24, 2014