10 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BD MAX STAPHSR ASSAY, INSTRUMENT
FDA 510(k)
FDA Class 2
·Microbiology
Portex
FDA UDI
ICU MEDICAL, INC.·15019517075625·
ASAP SINUSCOPE 10-0036-00,10-0037-00,10-0038,10-0039-00,10-0040-00,10-0041-00,10-0042-00,10-0043-00,10-0044-00,10-0045-0
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
IMPLANT-ONE SYSTEM
FDA 510(k)
FDA Class 2
·Dental
V 3.0 FIRM EXT
FDA Adverse Event
Death
·CONCENTRIC MEDICAL·Product code NRY·May 29, 2013
ESTEEM 1 PC - 1 PC DRAINABLE INVISICLOSE DRAINABLE POUCH - APS
FDA Adverse Event
Injury
·CONVATEC DOMINICAN REPUBLIC, INC.·Product code EZQ·September 29, 2014
COLLEAGUE PRE P1.7
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 17, 2011
HLM TUBING SET W/SOFTLINE COATING
FDA Adverse Event
Injury
·MAQUET CARDIOPULMONARY AG·Product code DTZ·November 18, 2015
HLM TUBING SET W/SOFTLINE COATING
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·June 3, 2016
HLM TUBING SET W/BIOLINE COATING
FDA Adverse Event
Malfunction
·MAQUET CARDIOPULMONARY AG·Product code DTZ·August 2, 2016