1,289 results
·
29ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
Ritter Implants Dental System
FDA UDI
Ritter Implants GmbH & Co. KG·ERITHDH1·
HDH Treatment Planning System
FDA 510(k)
FDA Class 2
·Dental
MCGHAN
FDA Adverse Event
Injury
·MCGHAN MED CORP.·Product code FWM·September 13, 1996
SINUS CURETTE B-6 HD H/O HANDLE
FDA UDI
W.H. Holden, Inc.·D928105119HO0·
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·May 7, 2018
AXSYM PROLACTIN REAGENT
FDA Adverse Event
Injury
·ABBOTT LABORATORIES·Product code CFT·March 14, 1997
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·October 15, 2025
BD TEXIUM CLOSED MALE LUER WITH FEMALE CAP
FDA Adverse Event
Malfunction
·SISTEMAS MEDICOS ALARIS S.A DE C.V.·Product code FPA·October 15, 2025
PALINDROME
FDA Adverse Event
Malfunction
·COVIDIEN LLC·Product code MSD·July 30, 2024
COREVALVE TRANSCATHETER AORTIC VALVE
FDA Adverse Event
Injury
·MEDTRONIC HEART VALVES DIVISION·Product code NPT·March 5, 2019
MERSILENE SURGICAL LIGATURE
FDA Adverse Event
Injury
·ETHICON, INC.·Product code HDH·December 1, 2016
CERVIX NEEDLE
FDA Adverse Event
Malfunction
·ETHICON, INC.·Product code HDH·August 2, 2000
AUTOSUTURE COMPANY
FDA Adverse Event
Injury
·AUTOSUTURE COMPANY·Product code HDH·May 12, 1994
HEARTMATE 3 LVAS IMPLANT KIT
FDA Adverse Event
Death
·THORATEC CORPORATION·Product code DSQ·November 12, 2021
UNSPECIFIED BD MICROFINE PLUS PEN NEEDLE
FDA Adverse Event
Malfunction
·BECTON DICKINSON·Product code FMI·February 18, 2021
Needle, Cerclage, Gynecological
FDA classification
FDA Class 1
·Needle, Cerclage, Gynecological
HBH MEDIZINTECHNIK GMBH
FDA registration
HBH MEDIZINTECHNIK GMBH·5 products·🇩🇪 Germany
HBH BIOTECHNOLOGY LIMITED
FDA registration
HBH BIOTECHNOLOGY LIMITED·6 products·🇨🇳 China
ADHE-ELS INTERNATIONAL
FDA registration
ADHE-ELS INTERNATIONAL·1 product·🇹🇳 Tunisia
HDA TECHNOLOGY, INC.
FDA registration
HDA TECHNOLOGY, INC.·2 products·🇺🇸 United States