11 results
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39ms
·
Sources: EU EUDAMED, US FDA
TriniCAL Reference Plasma
FDA registration
DIAGNOSTICA STAGO, INC.·1 product·🇺🇸 United States
TriniCAL Reference Plasma
FDA registration
TCOAG IRELAND LIMITED·1 product·🇮🇪 Ireland
VERIFY REFERENCE PLASMA AND MDA VERIFY REF. PLASMA
FDA 510(k)
FDA Class 2
·Hematology
System, Multipurpose For In Vitro Coagulation Studies
FDA classification
FDA Class 2
·System, Multipurpose For In Vitro Coagulation Studies
866062 IntelliVue Patient Monitor MX450
FDA registration
Philips Medizin Systeme Boeblingen GmbH·35 products·🇩🇪 Germany
866062 IntelliVue Patient Monitor MX450
FDA registration
Philips Electronics Ltd·35 products·🇨🇦 Canada
AmniSure ROM Test Positive and Negative Controls Pack
FDA registration
QIAGEN·2 products·🇺🇸 United States
INTELLIVUE PATIENT MONITOR MX400; INTELLIVUE PATIENT MONITOR MX450
FDA 510(k)
FDA Class 2
·Cardiovascular
AMNISURE FETAL MEMBRANES RUPTURE TEST MODEL FMRT1
FDA 510(k)
FDA Class 1
·Clinical Chemistry
Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
FDA classification
FDA Class 2
·Monitor, Physiological, Patient(With Arrhythmia Detection Or Alarms)
Single (Specified) Analyte Controls (Assayed And Unassayed)
FDA classification
FDA Class 1
·Single (Specified) Analyte Controls (Assayed And Unassayed)