9,000 results
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31ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
COBAS 6000 E601 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LJK·August 8, 2011
COBAS 6000 E601 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code LJK·October 4, 2011
PORT TITANIUM WITH GROSHONG
FDA Adverse Event
Malfunction
·DAVOL, INC.·Product code LJK·July 8, 1995
IMMULITE 2000
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LJK·October 28, 2013
Sekisui Diagnostics Ammonia L3K Assay; Catalog Number: 293-80-91 and 293-10 For the IN VITRO quantitative measurement of ammonia concentration in plasma
FDA Recall
Terminated
·Sekisui Diagnostics P.E.I. Inc.·Product code JIF·November 29, 2016
Antisera, If, Toxoplasma Gondii
FDA classification
FDA Class 2
·Antisera, If, Toxoplasma Gondii
CAPTURE-R READY-SCREEN 3
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·April 21, 2016
JLK, INC.
FDA registration
JLK, INC.·4 products·🇰🇷 South Korea
HU-FRIEDY
FDA UDI
HU-FRIEDY MFG. CO., LLC·10889950079536·LIGATURE DIRECTORS- DR. KNIGHT HANDEL#6
JLK-PWI
FDA UDI
JLK, Inc.·08800066200794·
JLK-ICH
FDA UDI
JLK, Inc.·08800066200589·
JLK-AILINK
FDA UDI
JLK, Inc.·08800066200619·
JLK-LVO
FDA UDI
JLK, Inc.·08800066200596·
JLK-SDH
FDA UDI
JLK, Inc.·08800066200602·
JLK-CTP
FDA UDI
JLK, Inc.·08800066200787·
LIK SANG OPTICAL FACTORY
FDA registration
LIK SANG OPTICAL FACTORY·2 products·🇭🇰 Hong Kong
RadiForce®
FDA UDI
EIZO CORPORATION·04995047059752·2MP Multitouch Color LCD Monitor
RadiForce®
FDA UDI
EIZO CORPORATION·04995047050919·2MP Multitouch Color LCD Monitor
MEDIHUB PROSTATE
FDA UDI
JLK, Inc.·08800066200626·
JLK-PWI
FDA 510(k)
FDA Class 2
·Radiology