9 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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MODEL ELI 100 ELECTROCARDIOGRAPH
FDA 510(k)24M - 16 person Class A First Aid/Burn Kit
FDA UDI
Certified Safety Manufacturing, Inc.·00766588206271·24M - 16 person Class A First Aid/Burn Kit
MICROSCAN MICROSTREP PLUS PANEL NEW ANTIMICROBIAL-GATIFLOXACIN
FDA 510(k)
FDA Class 2
·Microbiology
TOSHIBA 1.5T QD HEAD COIL
FDA 510(k)
FDA Class 2
·Radiology
E-CAM COINCIDENCE MODE [510 (K) K970627)
FDA Adverse Event
Malfunction
·SIEMENS MEDICAL SYSTEMS, INC., NMG GROUP·Product code IYX·April 20, 2001
TENSION FREE VAGINAL TAPE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code OTN·January 17, 2013
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·December 13, 2010
SUSTAIN XL DR
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code DXY·July 8, 2014
BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended for the qualitative detection of nucleic acid from the SARS-CoV-2 in nasopharyngeal specimens Catalog Number: 444213
FDA Enforcement
Class II
·Terminated·Becton Dickinson & Co.·April 21, 2021