60 results
·
23ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970584·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970591·
MAMMOTOME REOLVE DUAL VACUUM ASSISTED BIOPSY (VAB) SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
ArgenPMMA 95x30-C1
FDA UDI
ARGEN CORPORATION, THE·D818123259·Crown And Bridge, Temporary, Resin
Rumex
FDA UDI
RUMEX INTERNATIONAL CORP.·00840159901021·Pick Vitreoretinal Forceps, 25 Ga, Tip Only
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970423·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970126·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970393·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970416·
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970409·
INHEALTH SOFT SLEEVE COLONOSCOPE SPLINT, MODEL CS1200
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
NOTOUCH BREASTSCAN
FDA 510(k)
FDA Class 1
·Obstetrics/Gynecology
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·April 12, 2024
DAILY ACTIVITY ASSIST DEVICES
FDA Adverse Event
UNKNOWN·Product code ILS·May 21, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·September 26, 2014
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL, INC.·Product code NIK·June 14, 2011
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025
BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B CLIA-WAIVED KIT
FDA Adverse Event
Malfunction
·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·September 3, 2025