3,684 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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DADE® THROMBIN REAGENT
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code KQJ·July 25, 2024
OWREN'S VERONAL BUFFER
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code KQJ·September 14, 2021
MULTIFIBREN U
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code KQJ·April 4, 2019
MULTIFIBRIN U
FDA Adverse Event
Malfunction
·DADE BEHRING GMBH·Product code KQJ·September 18, 2007
DADE THROMBIN REAGENT
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code KQJ·October 23, 2024
MULTIFIBRIN U
FDA Adverse Event
Malfunction
·SIEMENS HEALTHCARE DIAGNOSTICS PRODUCTS GMBH·Product code KQJ·June 19, 2015
Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company LLC ,a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA --- For determination of Fibrinogen Degradation products in serum and urine.
FDA Recall
Terminated
·Fisher Diagnostics·Product code KQJ·May 19, 2017
Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scientific Company, LLC, a part of Thermo Fisher Scientific Inc., Middletown, VA 22645-1905 USA
FDA Recall
Terminated
·Fisher Diagnostics·Product code KQJ·May 19, 2017
STA - Fibrinogen 5. Model/Catalog Number: 00674. The STA - Fibrinogen 5 kit is intended for use with the analyzers of the STA-R, STA Compact and STA Satellite families for the quantitative determination of fibrinogen levels in human citrated plasma by the clotting method of Clauss.
FDA Recall
Open, Classified
·Diagnostica Stago, Inc.·Product code KQJ·July 21, 2025
System, Fibrinogen Determination
FDA classification
FDA Class 2
·System, Fibrinogen Determination
KimTrac
FDA UDI
B& L Biotech, inc.·08800019110620·
Capital
FDA UDI
COLLEGE PARK INDUSTRIES, INC.·00195411108381·Knee Pad Replacement Kit, Jet Black
NA
FDA UDI
Fehling Instruments GmbH & Co. KG·04058749024555·TC Wire twisting forceps 185 mm
KTJ DENTAL LAB INC
FDA registration
KTJ DENTAL LAB INC·10 products·🇺🇸 United States
KTJ-20C BLOOD PRESSURE CUFF, MODEL KTJ-20C
FDA 510(k)
FDA Class 2
·Cardiovascular
KTJ DENTAL LAB COMPANY LIMITED
FDA registration
KTJ DENTAL LAB COMPANY LIMITED·11 products·🇭🇰 Hong Kong
KTJ Medical Technology Co.,Ltd.
FDA registration
KTJ Medical Technology Co.,Ltd.·11 products·🇨🇳 China
MULTIPLE, MODEL KTJ-50
FDA 510(k)
FDA Class 2
·Cardiovascular
KJ MEDITECH CO., LTD.
FDA registration
KJ MEDITECH CO., LTD.·4 products·🇰🇷 South Korea
KDJ
FDA Adverse Event
Injury
·BAXTER HEALTHCARE·Product code KDJ·April 15, 2013