114 results
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64ms
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Sources: EU EUDAMED, US FDA
USA SCIENTIFIC, INC.
FDA registration
USA SCIENTIFIC, INC.·1 product·🇺🇸 United States
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FDA UDI
Usa Scientific, Inc.·00850064227048·Layer4 Comfort Nitrile Exam Gloves Medium 200 p...
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FDA UDI
Usa Scientific, Inc.·00850064227062·Layer4 Comfort Nitrile Exam Gloves Large 200 pe...
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FDA UDI
Usa Scientific, Inc.·00850064227024·Layer4 Comfort Nitrile Exam Gloves Small 200 pe...
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FDA UDI
Usa Scientific, Inc.·00850064227017·Layer4 Comfort Nitrile Exam Gloves X-Small 200 ...
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FDA UDI
Usa Scientific, Inc.·00850064227123·Layer4 RapidDon Nitrile Exam Gloves Small 250 p...
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FDA UDI
Usa Scientific, Inc.·00850064227185·Layer4 RapidDon Nitrile Exam Gloves X-Large 230...
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FDA UDI
Usa Scientific, Inc.·00850064227086·Layer4 Comfort Nitrile Exam Gloves X-Large 200 ...
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FDA UDI
Usa Scientific, Inc.·00850064227109·Layer4 RapidDon Nitrile Exam Gloves X-Small 250...
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FDA UDI
Usa Scientific, Inc.·00850064227161·Layer4 RapidDon Nitrile Exam Gloves Large 250 p...
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FDA UDI
Usa Scientific, Inc.·00850064227147·Layer4 RapidDon Nitrile Exam Gloves Medium 250 ...
Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company, LLC, a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA
FDA Enforcement
Class II
·Terminated·Fisher Diagnostics·August 2, 2017
Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company LLC ,a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA --- For determination of Fibrinogen Degradation products in serum and urine.
FDA Enforcement
Class II
·Terminated·Fisher Diagnostics·August 2, 2017
ZILVER FLEX 35 VASCULAR SELF-EXPANDING STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIO·July 27, 2022
ZILVER FLEX 35 VASCULAR SELF-EXPANDING STENT
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code NIO·July 27, 2022
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Injury
·COOK IRELAND LTD·Product code FGE·January 29, 2020
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code KRD·November 13, 2019