672 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075281491·Nextend | Lite
LG-272-N-PL
FDA UDI
LASER PERIPHERALS, LLC·00816469021520·LaseGuide® Nav 272u Laser Fiber PL
EVIS EXERA II COLONOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDF·April 19, 2024
EVIS EXERA III COLONOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDF·April 19, 2024
EVIS EXERA II COLONOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDF·April 19, 2024
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDS·April 19, 2024
LG-272-N-PL-M
FDA UDI
LASER PERIPHERALS, LLC·00816469021537·LaseGuide® Nav 272u Laser Fiber PL
HUMAPEN LUXURA BURGUNDY
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·October 27, 2016
HUMAPEN LUXURA HALF-DOSE PEN
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·October 30, 2015
BoneFoam
FDA UDI
BONE FOAM, INC.·00810075281521·Nextend | Lite | Single Use Kit | Box of 5
HUMAPEN UNKNOWN DEVICE
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·May 3, 2022
HUMAPEN LUXURA CHAMPAGNE
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·April 13, 2016
PENTAX
FDA Adverse Event
Malfunction
·HOYA CORPORATION PENTAX TOKYO OFFICE·Product code EQN·January 10, 2020
HUMAPEN ERGO, TEAL/CLEAR
FDA Adverse Event
Injury
·ELI LILLY AND CO.·Product code FMF·February 20, 2008
HUMAPEN ERGO BURGUNDY/CLEAR
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code NSC·February 17, 2010
HUMAPEN LUXURA BURGUNDY
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·September 10, 2015
HUMAPEN ERGO II
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·November 10, 2020
HUMAPEN ERGO II
FDA Adverse Event
Injury
·ELI LILLY AND COMPANY·Product code FMF·November 10, 2020
HUMAPEN ERGO, TEAL/CLEAR/CLEAR CH
FDA Adverse Event
Injury
·ELI LILLY AND CO.·Product code FMF·October 22, 2007
XEN 45 GTS (AUSTRALIA)
FDA Adverse Event
Injury
·ALLERGAN (AUSTIN)·Product code KYF·March 25, 2020