454 results
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30ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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Quadrox iD w RF 32 Pack
FDA UDI
DATASCOPE CORP.·00607567205758·BO-HMOD 70000-USA Adult Quadrox iD,
BO-RF32 Rot...
ECC 1/4" Quadrox iD w/RF
FDA UDI
DATASCOPE CORP.·00607567212374·BEQ-HMOD 70000-USA Adult Quadrox iD, Softshell ...
ECC Quadrox iD w/RF 3/8"
FDA UDI
DATASCOPE CORP.·00607567208544·BEQ-HMOD 70000-USA Adult Quadrox iD
Softshell V...
ECC Quadrox iD w/ RF 3/8"
FDA UDI
DATASCOPE CORP.·00607567212367·BEQ-HMOD 70000-USA Adult Quadrox iD, Softshell ...
CATHETER STABILIZATION, PICC/CENTRAL LINE
FDA Adverse Event
Malfunction
·C.R. BARD, INC. (BASD) -3006260740·Product code KMK·April 30, 2025
Maquet Getinge-BEQ-TOP 21502 ECC Quadrox iD w/RF 3/8" Material:701050060R01
FDA Recall
Terminated
·Maquet Cardiovascular, LLC·Product code DWF·April 18, 2019
SYNCHROMED EL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·February 6, 2008
Maquet Getinge-BEQ-TOP 21502 ECC Quadrox iD w/RF 3/8" Material:701050060R01
FDA Enforcement
Class II
·Terminated·Maquet Cardiovascular, LLC·June 5, 2019
PARFIN CUTTER/DISPENSER
FDA Adverse Event
Injury
·THERMO SEPERATION PRODUCTS·Product code IDW·November 20, 1994
UNK
FDA Adverse Event
Injury
·OLYMPUS AMERICA, INC.·Product code IDW·March 30, 2000
DISPENSERS, PARAFFIN
FDA Adverse Event
Malfunction
·LEICA MICROSYSTEMS LTD. SHANGHAI·Product code IDW·March 18, 2024
HISTOCORE ARCADIA H
FDA Adverse Event
Malfunction
·LEICA BIOSYSTEMS NUSSLOCH GMBH·Product code IDW·March 21, 2024
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·June 18, 2025
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·June 18, 2025
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·June 18, 2025
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·June 18, 2025
HEMODIALYSIS BLOODLINES
FDA Adverse Event
Malfunction
·B. BRAUN MEDICAL INC.·Product code FJK·June 18, 2025
CAPTURE-R READY-SCREEN (3)
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·April 26, 2012
SYNCHROMED EL
FDA Adverse Event
Injury
·MEDTRONIC NEUROMODULATION·Product code LKK·February 6, 2008
AXIUM PRIME BRPL 3D
FDA Adverse Event
Malfunction
·MICRO THERAPEUTICS, INC. DBA EV3·Product code KRD·April 9, 2021