603 results
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25ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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KIWI
FDA Adverse Event
Malfunction
·CORTEX·Product code HCJ·July 8, 2024
Device, Skin Potential Measurement
FDA classification
FDA Class 2
·Device, Skin Potential Measurement
CHJ
FDA registration
CHJ·3 products·🇯🇵 Japan
HCM MEDICAL
FDA registration
HCM MEDICAL·2 products·🇳🇱 Netherlands
HC-1 AND HC-1 CLASSIC
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Hypertec HCM LLC
FDA registration
Hypertec HCM LLC·19 products·🇺🇸 United States
HCI CO.,LTD
FDA registration
HCI CO.,LTD·1 product·🇰🇷 South Korea
LARS ACJ
FDA 510(k)
FDA Class 2
·Orthopedic
SOF-GEAR CHIN CUP WITH HEADCAP, JUNIOR
FDA UDI
G & H Wire Company, Inc.·10190886000434·An ultra-comfortable and effective headcap plus...
N/A
FDA UDI
Flexmedics·10195291009140·SG CHIN CUP W/JR HEADCAP
DAU HC 1
FDA UDI
UTAK LABORATORIES, INC.·B800507000·DAU HC 1
DAU HC 2
FDA UDI
UTAK LABORATORIES, INC.·B800507010·DAU HC 2
TrueStim
FDA UDI
Hi-Dow International Incorporated·00851640007139·Wired Classic Stimulation System BLACK
TrueStim
FDA UDI
Hi-Dow International Incorporated·00851640007122·Wired Classic Stimulation System WHITE
Subdural Electrode
FDA UDI
Ad-Tech Medical Instrument Corporation·00841823103734·
hc2 HPV DNA Test
FDA UDI
QIAGEN SCIENCES INC.·04053228002024·digene® HC2 HPV DNA Test (Low-Risk HPV and High...
HCA Edmond Manifold Kit
FDA UDI
ARGON MEDICAL DEVICES, INC.·00886333207916·HCA Edmond Manifold Kit
directCHECK Whole Blood Controls
FDA UDI
ACCRIVA DIAGNOSTICS HOLDINGS, INC.·10711234540046·Protective Sleeves
ASAHI PTCA GUIDE WIRE, FIELDER FC J, MODELS: AGP140001J, AGP140301J
FDA 510(k)
FDA Class 2
·Cardiovascular
hc2 High-Risk HPV DNA Test
FDA UDI
QIAGEN SCIENCES INC.·04053228002000·digene® HC2 High-Risk HPV DNA Test (4-Plate Kit)