10,000 results
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41ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·December 27, 2012
POWERED WHEELCHAIR
FDA Adverse Event
Malfunction
·INVACARE TAYLOR STREET·Product code ITI·July 26, 2012
TINA-QUANT ANTISTREPTOLYSIN O
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GTQ·August 12, 2024
SYNCHRON® ANTISTREPTOLYSIN-O (ASO) REAGENT
FDA Adverse Event
Malfunction
·BECKMAN COULTER, INC.·Product code GTQ·July 30, 2011
TINA-QUANT ANTISTREPTOLYSIN O
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GTQ·June 23, 2025
ASLOT TINA-QUANT ANTISTREPTOLYSIN O
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GTQ·April 3, 2017
TINA-QUANT ANTISTREPTOLYSIN O
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code GTQ·April 14, 2025
DIFCO Laboratories, FA Streptococcus Group A, 5mL, Catalog Number: 223181, Lot number: 6122656, Exp: 20090705, in vitro diagnostic.
FDA Recall
Terminated
·BD Diagnostic Systems Lee Laboratories·Product code GTQ·August 8, 2007
Remel Staphaurex Plus Kit, Catalog No. R30950102 (150 tests) and Catalog No. R30950201 (450 tests), rapid latex agglutination test for the identification of Staphylococcus aureus The responsible firm listed as Remel Europe Ltd, Dartford, England.
FDA Recall
Terminated
·Remel, Inc·Product code GTQ·November 18, 2008
Array Systems Calibrator 5 Part No. 465250
FDA Recall
Terminated
·Beckman Coulter Inc·Product code GTQ·December 17, 2003
Roche Tina-Quant ASLO (Anti-streptolysin O) Reagent Kit; Catalog No. 1931601 (Roche Material No. 11931601216) Lot No. 674653
FDA Recall
Terminated
·Roche Diagnostics Corp.·Product code GTQ·July 25, 2006
Antistreptolysin - Titer/Streptolysin O Reagent
FDA classification
FDA Class 1
·Antistreptolysin - Titer/Streptolysin O Reagent
GT2 HEALTHCARE SDN.BHD.
FDA registration
GT2 HEALTHCARE SDN.BHD.·1 product·🇲🇾 Malaysia
GTI MEDICAL LTD
FDA registration
GTI MEDICAL LTD·1 product·🇮🇱 Israel
GT1 FLOPPY, GT1 HI-PER FLEX, GT1 LIGHT SUPPORT
FDA 510(k)
FDA Class 2
·Cardiovascular
Immucor GTI Diagnostics, Inc.
FDA registration
Immucor GTI Diagnostics, Inc.·5 products·🇺🇸 United States
Ultrasonic transducer
FDA UDI
Edan Instruments, Inc.·06944413809055·
DRIVER HANPIECE SQUARE 30
FDA UDI
Sin Sistema de Implante Nacional S/A·07899995206381·DRIVER HANPIECE SQUARE 30
DRIVER HANPIECE SQUARE 20
FDA UDI
Sin Sistema de Implante Nacional S/A·07899995206312·DRIVER HANPIECE SQUARE 20
INVACARE® 3G STORM SERIES® TORQUE™ SP POWER WHEELCHAIR
FDA UDI
INVACARE CORPORATION·00841447100935·