49 results
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54ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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ENDO TECH INSTRUMENTS
FDA registration
ENDO TECH INSTRUMENTS·61 products·🇵🇰 Pakistan
ENDO GIA STAPLER LOAD
FDA Adverse Event
Malfunction
·COVIDIEN (UNITED STATES SURGICAL CORP)·Product code GDW·September 29, 2008
ENDO GIA AUTOSUTURE GUN
FDA Adverse Event
Malfunction
·US SURGICAL CORP·Product code GAG·July 22, 1993
ENDO STITCH* 10MM SUTURING DEVICE
FDA Adverse Event
Malfunction
·COVIDIEN·Product code KOG·October 17, 2016
P.E.E.R. RETRACTOR, ROTO-LOK, RATCHET, 10MM, 32CM
FDA Adverse Event
Injury
·TONTARRA MEDIZINTECHNIX·Product code KOG·August 15, 2006
ENDO STITCH* SURGIDAC*2/0 48 GRN DLU SU
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code OCW·July 13, 2015
RX LOCKING DEVICE AND BIOPSY CAP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code ODC·October 3, 2024
EGIA 30 ARTICULATING MED/THICK SULU
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·November 25, 2015
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GDO·December 20, 1999
LIGACLIP ENDOSCOPIC ROTATING MULTIPLE CLIP APPLIER
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC.·Product code GDO·December 20, 1999
EGIA ULTRA UNIVERSAL XL STAPLER
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL·Product code GDW·June 19, 2013
POWERED 60 ECHELON +, 340MM SHAFT
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·March 23, 2021
BIPOLAR TRL RETAINING CLIP 28
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code LXH·October 22, 2020
MULTIFIRE ENDO GIA
FDA Adverse Event
Malfunction
·US SURGICAL PUERTO RICO·Product code GDW·October 6, 2017
RX LOCKING DEVICE AND BIOPSY CAP
FDA Adverse Event
Malfunction
·BOSTON SCIENTIFIC CORPORATION·Product code ODC·September 11, 2024
ETS FLEX ARTICNG LNR CUTR 45MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 18, 2023
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·February 3, 2023
BIPOLAR TRL RETAINING CLIP 28
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code LXH·October 21, 2020
S/C & MOD CATH TRL 45/28
FDA Adverse Event
Malfunction
·DEPUY ORTHOPAEDICS INC US·Product code LXH·January 7, 2021
EGIA 60 ARTICULATING MED/THICK SULU
FDA Adverse Event
Malfunction
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GDW·June 3, 2016