10,000 results
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58ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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BAOT
FDA UDI
BAOT Biological Technology Co., Ltd.·06973133311913·Dental Ceramic is indicated for use for metal-c...
BAOT
FDA UDI
BAOT Biological Technology Co., Ltd.·06973133312132·Dental Ceramic is indicated for use for metal-c...
JCM LABS CUSTOM PRESCRIPTION & ACCENT IN-THE-EAR
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
ARROW
FDA UDI
TELEFLEX INCORPORATED·30801902120206·Pneumothorax
ARROW
FDA UDI
TELEFLEX INCORPORATED·10801902120202·Pneumothorax Kit with Sharps Safety Features
ARROW
FDA UDI
TELEFLEX INCORPORATED·20801902053279·Pneumothorax Kit
ARROW
FDA UDI
TELEFLEX INCORPORATED·00801902053275·Pneumothorax Kit with Sharps Safety Features
MICROSCAN DRIED GRAM NEGATIVE ID PANELS
FDA Adverse Event
Malfunction
·DADE BEHRING, INC.·Product code LRG·October 21, 2003
DURATA
FDA Adverse Event
Injury
·ABBOTT·Product code NVY·October 30, 2019
OPTIGUIDE FIBER OPTIC DIFFUSER
FDA Adverse Event
Injury
·PINNACLE BIOLOGICS INC·Product code MVG·October 15, 2025
BBLS
FDA Adverse Event
Injury
·SCITON INC.·Product code GEX·July 7, 2025
VITEK 2
FDA Adverse Event
Malfunction
·BIOMERIEUX, INC.·Product code JTN·May 2, 2006
DURATA
FDA Adverse Event
Malfunction
·ABBOTT·Product code LWS·December 20, 2019
SICKLEDEX
FDA Adverse Event
Malfunction
·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JCM·November 29, 2005
2250051-2005-00561
FDA Adverse Event
Malfunction
·Product code JCM·November 29, 2005
LIGHT SHEER EC
FDA Adverse Event
Injury
·LUMENIS LASERS, INC.·Product code GEX·March 22, 2002
OPEN PIVOT STANDARD AORTIC HEART VALVE
FDA Adverse Event
Injury
·MEDTRONIC, INC.·Product code LWQ·November 8, 2017
LASER APPLICATOR
FDA Adverse Event
Injury
·CHATTANOOGA GROUP·Product code ILY·June 5, 2009
DRIVER RX
FDA Adverse Event
Death
·MEDTRONIC IRELAND·Product code MAF·January 20, 2018
VECTRA GENISYS LASER
FDA Adverse Event
Injury
·CHATTANOOGA GROUP·Product code ILY·June 5, 2009