191 results
·
20ms
·
Sources: EU EUDAMED, US FDA
AMEDICA DRUG SCREEN METHAPHETAMINE TEST
FDA 510(k)
FDA Class 2
·Clinical Toxicology
PERMITE
FDA UDI
SDI LIMITED·DO3640231012·
Ophthalmic Cannula
FDA UDI
KATENA PRODUCTS, INC.·00841668113776·AIR INJECT CANNULA 27GA
N/A
FDA UDI
BIOMET MICROFIXATION, INC·00888233025164·
ALLOGENIX
FDA UDI
BIOMET MICROFIXATION, INC·00841036125844·
NA
FDA UDI
STERILMED, INC.·10888551017756·SAW BLADE INTRA ORAL COARSE
MICROCHOICE
FDA UDI
Conmed Corporation·10845854006627·MICROCHOICE OSCILLATOR INTRA-ORAL BLADE 11.5 X ...
MEDTEXX POWDERFREE NITRILE RUBBER EXAMINATION GLOVES, GREEN COLOUR
FDA 510(k)
FDA Class 1
·General Hospital
WIENER LAB. AMILASA 405 CINETICA AA, WIENER LAB.AMILASA 405 CINETICA UNITEST,WIENER LAB.AMILASA CINETICA AA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
ORTHO SUMMIT SAMPLE HANDLING SYSTEM
FDA Adverse Event
Malfunction
·HAMILTON BONADUZ AG·Product code JTC·February 1, 2000
PLUM A+3 V11.51 REFR
FDA Adverse Event
Malfunction
·HOSPIRA COSTA RICA LTD.·Product code FRN·February 26, 2013
LEAD NEURO
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LGW·February 24, 2011
COLLEAGUE CX VOLUMETRIC INFUSION PUMP
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE PTE LTD·Product code FRN·April 3, 2008
WATCHMAN FLX LEFT ATRIAL APPENDAGE CLOSURE DEVICE WITH DELIVERY SYSTEM
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC CORPORATION·Product code NGV·May 24, 2023
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·January 12, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 2, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·April 6, 2026
PANEL PHOENIX PMIC-110
FDA Adverse Event
Malfunction
·BECTON DICKINSON & CO. (SPARKS)·Product code LON·March 30, 2026
EVIS EXERA III DUODENOVIDEOSCOPE
FDA Adverse Event
Injury
·AIZU OLYMPUS CO., LTD.·Product code FDT·August 19, 2025