1,012 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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HnX-P1, HnX-PB
FDA 510(k)
FDA Class 2
·Radiology
HnX-PB
FDA UDI
H&abyz Co., Ltd·08800070400166·The portable x-ray system may be used for diagn...
HnX-P1
FDA UDI
H&abyz Co., Ltd·08800070400074·The portable x-ray system may be used for diagn...
STORZ SPAINDE SCLERAL DEPRESSOR
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, INC.·Product code HNX·February 1, 2012
FLYNN SCLERAL DEPRESSOR
FDA Adverse Event
Injury
·BAUSCH & LOMB SURGICAL·Product code HNX·August 2, 2000
SCLERAL DEPRESSOR
FDA Adverse Event
Malfunction
·STORZ OPTHALMICS·Product code HNX·September 21, 2011
SPAIDE PEDIATRIC SCLERAL DEPRESSOR
FDA Adverse Event
Malfunction
·BAUSCH & LOMB, STORZ OPHTHALMICS·Product code HNX·December 8, 2011
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HNX·January 30, 2019
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·DEPUY MITEK LLC US·Product code HNX·June 26, 2018
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·Product code HNX·September 25, 2019
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·Product code HNX·September 13, 2019
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·Product code HNX·September 13, 2019
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·Product code HNX·September 25, 2019
1392 5.9MM STRYKER SHEATH 2 WAY -NS
FDA Adverse Event
Malfunction
·Product code HNX·September 25, 2019
Depressor, Orbital
FDA classification
FDA Class 1
·Depressor, Orbital
BNX
FDA UDI
Covidien LP·00855208005025·FINE NEEDLE ASPIRATION SYSTEM
BNX
FDA UDI
Covidien LP·00855208005070·FINE NEEDLE ASPIRATION NEEDLE
BNX
FDA UDI
Covidien LP·00855208005049·FINE NEEDLE ASPIRATION SYSTEM
HDX WILL CORP.
FDA registration
HDX WILL CORP.·6 products·🇰🇷 South Korea
ANX ROBOTICA CORP.
FDA registration
ANX ROBOTICA CORP.·6 products·🇺🇸 United States