7 results
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22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CONCHATHERM IV HEATED MOLECULAR HUMIDIFIER
FDA 510(k)
FDA Class 2
·Anesthesiology
ACON ONE STEP MULTI-DRUG MULTI-LINE SCREEN TEST CARD, ACON ONE STEP MULTI-DRUG MULTI-LINE SCREEN TEST DEVICE
FDA 510(k)
FDA Class 2
·Clinical Toxicology
WARMAIR MODEL 135 HYPERTHERMIA SYSTEM INCLUDING FILTEREDFLO BLANKETS
FDA 510(k)
FDA Class 2
·Cardiovascular
MULTI-DRUG ONE STEP SCREEN TEST PANEL (URINE)
FDA Adverse Event
Malfunction
·ABON BIOPHARM (HANGZHOU) CO., LTD.·Product code LFG·April 1, 2024
PROSIMA PELVIC FLOOR REPAIR KIT
FDA Adverse Event
Injury
·ETHICON,INC.·Product code FTL·January 22, 2013
3005075853-2010-05501
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·December 14, 2010
QUICKFLEX MICRO LV LEAD
FDA Adverse Event
Injury
·ST. JUDE MEDICAL, INC., CRMD·Product code OJX·July 9, 2014