179 results
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24ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MANATEC
FDA registration
MANATEC·1 product·🇫🇷 France
PhysioFlow
FDA UDI
MANATEC·03760125071046·
PhysioFlow
FDA UDI
MANATEC·03760125071152·
PhysioFlow
FDA UDI
MANATEC·03760125071213·
MAWATEC AG
FDA registration
MAWATEC AG·7 products·🇨🇭 Switzerland
Facet Manatee Reusable Lancing Base
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ELA MEDICAL ANATEC HOLTER SCANNER
FDA 510(k)R82
FDA UDI
R82 A/S·05707292386861·
R82
FDA UDI
R82 A/S·05707292386908·
R82
FDA UDI
R82 A/S·05707292386915·
R82
FDA UDI
R82 A/S·05707292386878·
R82
FDA UDI
R82 A/S·05707292505125·
R82
FDA UDI
R82 A/S·05707292416704·
R82
FDA UDI
R82 A/S·05707292505132·
Ventyv
FDA UDI
SRI TRANG USA, INC.·00843013101100·
ATEC BIOPSY SYSTEM
FDA Adverse Event
Other
·HOLOGIC, INC.·Product code KNW·April 22, 2011
ATEC TRIMARK BIOPSY SITE IDENTIFICATION SYSTEM
FDA Adverse Event
Other
·HOLOGIC INC·Product code NEU·March 5, 2012
ATEC PEARL
FDA Adverse Event
Injury
·HOLOGIC, INC.·Product code KNW·July 7, 2022
ATEC 0914-20MR
FDA Adverse Event
Malfunction
·HOLOGIC, INC·Product code KNW·May 15, 2026
ATEC PEARL
FDA Adverse Event
Malfunction
·HOLOGIC, INC·Product code KNW·September 24, 2022