24 results
·
21ms
·
Sources: EU EUDAMED, US FDA
KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
PMMA disc
FDA UDI
Dentsply International Inc.·D00180722160·
Channel Drain
FDA UDI
C. R. Bard, Inc.·00801741049811·Channel Drain, 7mm Flat 3/4 Fluted with 4.7mm T...
Genius Total Knee System
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215021702·
LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 24, 2025
LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·December 23, 2025
NITRILE EXAMINATION GLOVE, PRE-POWDERED, COLOR WHITE
FDA 510(k)
FDA Class 1
·General Hospital
NIROYAL BILIARY PREMOUNTED STENT SYSTEM
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Crescendo Meniscal Insert CR Ultracongruent 12mm Size 6
FDA UDI
AMPLITUDE SAS·03701089524780·
BD SYRINGE 5ML LL EURO 125 S/C
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 27, 2026
BD SYRINGE 5ML LL EURO 125 S/C
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 27, 2026
BD SYRINGE 5ML LL EURO 125 S/C
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·February 27, 2026
WAVEWRITER ALPHA? PRIME 16
FDA Adverse Event
Injury
·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·November 4, 2025
DEXCOM G6 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·March 27, 2024
2.5MM TI ELASTIC NAIL 440MM
FDA Adverse Event
Malfunction
·SYNTHES USA·Product code HTY·April 23, 2013
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·April 28, 2011
CAPSURE SP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·July 10, 2008
LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 26, 2025
LUER-LOK
FDA Adverse Event
Malfunction
·BECTON DICKINSON MEDICAL SYSTEMS·Product code FMF·November 26, 2025
ESSURE
FDA Adverse Event
Injury
·BAYER PHARMA AG·Product code HHS·December 17, 2019