10 results
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23ms
·
Sources: EU EUDAMED, US FDA
GenPrime Snap-Top Split Key Cup
FDA 510(k)
FDA Class 2
·Clinical Toxicology
ForPro
FDA UDI
Tng Worldwide, Inc.·00672047101387·Blue Nitrile Glove
Size Medium
100ct
Biogel
FDA UDI
Bosma Enterprises·10818634023824·Biogel Skinsense Indicator Underglove Surgical ...
SOMATOM SENSATION 64 AND SENSATION CARDIAC
FDA 510(k)
FDA Class 2
·Radiology
MARROMAX B ONE MARROW ASPIRATION NEEDLE KIT, MODELS 50083-XX, 50084-XX
FDA 510(k)
FDA Class 2
·General Hospital
ASR ACETABULAR CUPS 50
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·May 31, 2013
GOBED II
FDA Adverse Event
Malfunction
·STRYKER MEDICAL·Product code FNL·June 15, 2011
STERRAD 200 STERILIZATION SYSTEM SINGLE-DOOR UNIT WITH STAINLESS STEEL EXTERIOR
FDA Adverse Event
Malfunction
·ADVANCED STERILIZATION PRODUCTS·Product code MLR·August 28, 2008
Retractor f/Sciatic Nerve Long; Part number: 03.100.014; UDI: 10886982070630
FDA Enforcement
Class II
·Terminated·Synthes (USA) Products LLC·May 16, 2018
PKG, MARYLAND FORCEPS, CURVED LEFT, P/N 0250080282. 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