9 results
·
25ms
·
Sources: EU EUDAMED, US FDA
EMIT-ST SERUM PHENOBARBITAL ASSAY
FDA 510(k)
FDA Class 2
·Clinical Toxicology
Marienfeld Superior
FDA UDI
Paul Marienfeld GmbH & Co. KG·04064279010500·
A-FIT®
FDA UDI
Gc Orthodontics America Inc.·E53581162100001·A-FIT® 1. MOLAR UPR RGT SZ 21
KOALA CLAMP, KOALA CLAMP AND CUTTER
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
MASIMO RESPOSABLE SPO2 SERIES OXIMETRY SENSORS, MASIMO LNCS / M-LNCS OXIMETRY SENSORS
FDA 510(k)
FDA Class 2
·Cardiovascular
OT VERIO PRO PLUS METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·May 15, 2014
VIRTUOSO VR
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code LWS·October 31, 2012
SAGB QUICK CLOSE
FDA Adverse Event
Malfunction
·OBTECH MEDICAL SARL_·Product code LTI·August 23, 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