9 results
·
26ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
MEDI
FDA UDI
MEDI MANUFACTURING, INC.·04051526799325·MANUMED ACTIVE WRIST LEFT SILVER M
VOLUSON E6, E8, E8 EXPERT, E10 DIAGNOSTIC ULTRASOUND SYSTEM
FDA 510(k)
FDA Class 2
·Radiology
GULLIVER AND CLASSE A
FDA 510(k)
FDA Class 1
·Dental
Xpert Xpress MVP, GeneXpert Dx System, GeneXpert Infinity System
FDA 510(k)
FDA Class 2
·Microbiology
BRAVO
FDA Adverse Event
Malfunction
·GIVEN IMAGING LTD.·Product code FFT·November 18, 2010
ASR ACETABULAR CUPS 46
FDA Adverse Event
Injury
·DEPUY INTERNATIONAL·Product code KWA·January 11, 2013
ACUITY
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code LWP·July 3, 2014
smiths medical Pneupac paraPAC plus 300 ventilator kit without PEEP and CPAP, REF P300NUS
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·March 27, 2024
paraPAC 300 ventilator kit without internal PEEP and CPAP, Item Number P300N
FDA Enforcement
Class I
·Ongoing·Smiths Medical ASD Inc.·October 2, 2024