1,107 results
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40ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Skytron
FDA UDI
SKYTRON LLC·10841736116385·Pullout keyboard 22 Inch, requires shelf for su...
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902131529·PI CVC KIT: 3-L 7 FR X 20 CM AGB+
ARROW
FDA UDI
TELEFLEX INCORPORATED·00801902089700·Pressure Injectable Multi-Lumen Central Venous ...
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902131512·PI CVC KIT: 3-L 7 FR X 16 CM AGB+
ARROW
FDA UDI
TELEFLEX INCORPORATED·00801902098832·Pressure Injectable Multi-Lumen Central Venous ...
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code ODG·September 3, 2021
ARROW CLAMP CATHETER COMPONENT
FDA Adverse Event
Death
·ARROW INTERNATIONAL INC.·Product code PUK·September 1, 2017
BIS
FDA Adverse Event
Malfunction
·JABIL CIRCUIT SINGAPORE PTE LTD·Product code OLW·August 3, 2022
BIS
FDA Adverse Event
Malfunction
·MMJ SA DE CV (USD)·Product code OLW·August 3, 2022
CYPASS SYSTEM
FDA Adverse Event
Malfunction
·TRANSCEND MEDICAL INC.·Product code OGO·July 19, 2018
HAHN TAPERED IMPLANT Ø3.5 X 11.5 MM
FDA Adverse Event
Malfunction
·PRISMATIK DENTALCRAFT, INC.·Product code DZE·November 23, 2023
CYPASS SYSTEM
FDA Adverse Event
Malfunction
·TRANSCEND MEDICAL INC.·Product code OGO·June 22, 2018
EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·May 5, 2021
Administration Set Securement Device
FDA classification
FDA Class 1
·Administration Set Securement Device
RONDO-PAK
FDA registration
RONDO-PAK·4 products·🇺🇸 United States
WATER PIK, INC.
FDA registration
WATER PIK, INC.·2 products·🇺🇸 United States
NUK USA LLC
FDA registration
NUK USA LLC·7 products·🇺🇸 United States
M-PAK, INC.
FDA registration
M-PAK, INC.·1 product·🇺🇸 United States
PAK TOOLS SURGICAL INSTRUMENTS
FDA registration
PAK TOOLS SURGICAL INSTRUMENTS·16 products·🇵🇰 Pakistan
Nice-Pak Products, LLC
FDA registration
Nice-Pak Products, LLC·1 product·🇺🇸 United States