33 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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NEWGEN/UNIVERSAL MANDIBULAR SYSTEM
FDA 510(k)
FDA Class 2
·Dental
SOLIDEA
FDA UDI
CALZIFICIO PINELLI SRL·08300496014263·NAOMI 100, SIZE M, SABBIA, GRADUATED COMPRESSIO...
Merit Medical®
FDA UDI
Merit Medical Systems, Inc.·00884450848203·
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH INC.·Product code QJR·February 8, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·June 3, 2021
ID NOW COVID 19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·June 2, 2021
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575581·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575598·
Navagio
FDA UDI
Kalitec Direct LLC·B07330K0142130·Trial, TLIF, 32L OB CRV 7Deg, 13mm
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575604·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575642·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575628·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575611·
BETHENNY EYEWEAR
FDA UDI
FGX INTERNATIONAL INC.·00193033575635·
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·June 3, 2021
ID NOW COVID-19 ASSAY
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·June 3, 2021
IDNOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 7, 2021
ID NOW COVID-19
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS SCARBOROUGH, INC.·Product code QJR·March 7, 2021
MARQUETTE EAGLE MONITOR MODEL 4000, MODEL N3024
FDA 510(k)
FDA Class 2
·Cardiovascular
REMSTAR PLUS CPAP SYSTEM
FDA 510(k)
FDA Class 2
·Anesthesiology