936 results
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22ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HNI
FDA UDI
G.L.E. Gesellschaft für lichttechnische Erzeugnisse mbH·04054657500075·UV - Tanning lamp, Accession # 0631196-001
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DISPOSABLE TWO-PART TROCAR NEEDLE
FDA Adverse Event
Malfunction
·COOK INC·Product code FBQ·December 19, 2018
STRAIGHT TROCAR SLEEVE
FDA Adverse Event
Injury
·RICHARD WOLF GERMANY (RWGMBH)·Product code FBQ·October 9, 2017
SEALING UNIT F/10/12MM TROCARS W.REDUCER
FDA Adverse Event
Injury
·AESCULAP AG·Product code FBQ·May 11, 2022
SEALING UNIT F/10/12MM TROCARS W.REDUCER
FDA Adverse Event
Injury
·AESCULAP AG·Product code FBQ·May 11, 2022
ENDOPATH TROCAR SHEATH
FDA Adverse Event
Injury
·ETHICON·Product code FBQ·February 4, 1994
ENDOPATH DISPOSABLE SURGICAL TROCAR AND SLEEVE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code FBQ·January 27, 1994
KARL STORZ SPATULA AND TROCAR
FDA Adverse Event
Other
·KARL STORZ GMBH & CO.·Product code FBQ·February 25, 1994
APPLIED MEDICAL
FDA Adverse Event
Malfunction
·APPLIED·Product code FBQ·December 24, 2009
ETHICON
FDA Adverse Event
Injury
·JOHNSON & JOHNSON·Product code FBQ·June 30, 1992
ETHICON ENDOPATH
FDA Adverse Event
Other
·ETHICON, INC.·Product code FBQ·February 13, 1995
ETHICON ENDOPATH 512 X AND 512S TROCARS
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY·Product code FBQ·January 18, 1995
UNIVERSAL REDUCER 5/10/12MM 3-HOLE
FDA Adverse Event
Malfunction
·CONMED CORP.·Product code FBQ·December 5, 2005
UNIVERSAL REDUCER 5/10/12MM
FDA Adverse Event
Malfunction
·CONMED CORPORATION·Product code FBQ·October 24, 2006
COOK BRAND TRANSEPTAL NEEDLE
FDA Adverse Event
Injury
·COOK, INC.·Product code FBQ·April 16, 2019
3.2MM PELLET INSERTION TRAY #2 - STERILE / LATEX FREE
FDA Adverse Event
Injury
·75 ARKAY DRIVE·Product code FBQ·September 28, 2024
LAPAROSCOPIC TROCAR SLEEVE W/CLIP VALVE
FDA Adverse Event
Malfunction
·RICHARD WOLF GMBH·Product code FBQ·November 10, 1993
AUTO SUTURE SURGIPORT
FDA Adverse Event
Injury
·UNITED STATES SURGICAL CORPORATION·Product code FBQ·February 19, 1992
SURGIPORT 10MM
FDA Adverse Event
Injury
·UNITED STATES SURGICAL CORPORATION·Product code FBQ·February 19, 1992
LAPAROSCOPIC TROCAR SLEEVE
FDA Adverse Event
Malfunction
·R WOLF, GMBH·Product code FBQ·August 5, 1994