10,000 results
·
21ms
·
Sources: EU EUDAMED, US FDA
SCINTILLATING FIBER DOSIMETER (SFD), MODEL MT-SFD-1000
FDA 510(k)
FDA Class 2
·Radiology
Scharioth IOL Scleral fixation forceps, straight & curved. (25 gauge / 0.5mm)
FDA UDI
D.O.R.C. Dutch Ophthalmic Research Center (International) B.V.·08717872017839·
SINUS DRILL
FDA UDI
OCO BIOMEDICAL INC·D78540SFD0·4.0 SINUS FLOOR DRILL
FLOOR DRILL
FDA UDI
OCO BIOMEDICAL INC·D78550SFD0·5.0 SINUS FLOOR DRILL
SEMELLE AVEC TUBE ACIER SF D
Device
EU MDR
·
Eu Md Class 1
·JANTON (G2M)·On the market·32 countries
MULTI-FORMAT SFD MODEL 1720
FDA 510(k)
FDA Class 2
·Radiology
SFD-035 SPOT FILM DEVICE
FDA 510(k)
FDA Class 2
·Radiology
SINGLE DISPOSABLE TRANSPAC IV TRANSDUCER
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code DRS·February 20, 1998
SINGLE DISPOSABLE TRANSPAC IV TRANSDUCER
FDA Adverse Event
Malfunction
·ABBOTT LABORATORIES·Product code DRS·February 20, 1998
PRESTILIX 1600X
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS EUROPE·Product code JAA·May 7, 2004
SPOT FILM DEVICE
FDA Adverse Event
Malfunction
·GE MEDICAL SYSTEMS·Product code JAA·March 26, 2003
SYRINGE 10ML LL W/TWINPAK DEVICE
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMI·April 28, 2021
GE Healthcare Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems. A universal diagnostic imaging system for radiographic and fluoroscopic examinations. Applications can be performed with the patient sitting, standing, or lying in the prone or supine position. Legacy and Legacy D Table is intended for use in a diagnostic X-ray system to support patient during general purpose radiological procedures in the horizontal, vertical and Trendelenburg positions.
FDA Recall
Terminated
·GE Healthcare·Product code JAA·June 12, 2015
ELECSYS TROPONIN T HS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code MMI·April 29, 2025
MODEL COLE TAB-2 TABLE W/MODEL COLE SFD-2 SPOTFILM
FDA 510(k)
FDA Class 2
·Radiology
CATHETER SMARTTOUCH THERMOCOOL SF D-F CURVE ABLATION BIDIRECTIONAL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code LPB·August 14, 2024
ELECSYS TROPONIN T HS
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code MMI·May 15, 2025
CATHETER SMARTTOUCH THERMOCOOL SF D-F CURVE ABLATION BIDIRECTIONAL
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC.·Product code LPB·August 14, 2024
THERMOCOOL SMARTTOUCH SF
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER INC·Product code LPB·November 22, 2024
COBAS 8000 E 801 MODULE
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code JJE·October 30, 2024