15 results
·
17ms
·
Sources: EU EUDAMED, US FDA
KALLESTAD QUANTITOPE LOW LEVEL IGE REAG
FDA 510(k)
FDA Class 2
·Immunology
Arx
FDA UDI
Life Spine, Inc.·00190837131579·
Arx
FDA UDI
Life Spine, Inc.·00190837172817·
Arx
FDA UDI
Life Spine, Inc.·00190837131562·
Arx
FDA UDI
Life Spine, Inc.·00190837131586·
Arx
FDA UDI
Life Spine, Inc.·00190837175757·
Arx
FDA UDI
Life Spine, Inc.·00190837190354·
Arx
FDA UDI
Life Spine, Inc.·00190837131555·
Arx
FDA UDI
Life Spine, Inc.·00190837188887·
VERDICT -II TCA, VERDICT-II MTD
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Hysteroscope System
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
ANIMAS VIBE
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 15, 2014
CONCERTO CRT-D DR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·October 31, 2012
ACCU-CHECK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS INC·Product code LZG·August 17, 2010
Unify, Sterile EO, Model #/ Part #: CD3231-40/100029240, 100030104, 100041904; CD3231-40Q/100029281, 100030124, 100041905; CD3235-40/100029256, 100029293, 100029307, 100031111, 100037047, 100048897, 100070009; CD3235-40Q/100029257, 100029294, 100029308, 100031059, 100037048, 100070010; CD3281-40Q/100056770; CD3297-40/100056933
FDA Enforcement
Class II
·Terminated·St Jude Medical Inc.·July 4, 2018