6,459 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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LEOPARD
FDA UDI
IMEDICOM CO., LTD.·08800038053151·Small Wrench
UNK HIP FEMORAL STEM ACTIS
FDA Adverse Event
Malfunction
·DEPUY IRELAND - 9616671·Product code LPH·May 11, 2026
Flat Fluted Drain 4x10 mm w/trocar
FDA UDI
REDAX SPA·08034139295084·A sterile and single-use silicone device charac...
NEOTRODE II - O
FDA Adverse Event
Other
·CONMED·Product code DRX·April 7, 1999
SEE H10
FDA Adverse Event
Malfunction
·BD INFUSION THERAPY SYSTEMS INC. S.A. DE C.V.·Product code FOZ·February 18, 2021
Thora Mayo Scs 10 mm w/wide blades
FDA UDI
SCANLAN INTERNATIONAL INC·00846159025385·Thoracoscopic Metz Scissors, 10mm, Wide Blades
*
FDA Adverse Event
BIOMET MICROFIXATION·Product code HWC·February 24, 2011
ENDOCLIP
FDA Adverse Event
Injury
·COVIDIEN·Product code FZP·October 3, 2014
20G X 1.16IN (1.1 X 30 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·August 2, 2019
22G X 0.75IN (0.7 X 19 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·April 30, 2019
24G X 0.75IN (0.7 X 19 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·September 23, 2019
20G X 1.16IN (1.1 X 30 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·December 5, 2019
18G X 1.16IN (1.3 X 30 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·September 18, 2019
24G X 0.75IN (0.7 X 19 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·September 23, 2019
Flat Drain type Jackson-Pratt 3x7 mm w/trocar
FDA UDI
REDAX SPA·08034139294537·The surgical drainage is a sterile and single-u...
20G X 1.16IN (1.1 X 30 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD (SUZHOU)·Product code FOZ·December 6, 2019
24G X 0.75IN (0.7 X 19 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·December 31, 2019
22G X 1.00IN (0.9 X 25 MM) W/ Y INTIMA II
FDA Adverse Event
Injury
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·July 10, 2019
20G X 1.16IN (1.1 X 30 MM) W/ Y INTIMA II
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code FOZ·January 22, 2020
HUDSON VENTILATOR TUBING SET, LONG LENGTH
FDA Adverse Event
Malfunction
·TELEFLEX MEDICAL·Product code BZO·November 7, 2013