12 results
·
22ms
·
Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
×
BPS Wrist Fracture System
FDA 510(k)
FDA Class 2
·Orthopedic
N/A
FDA UDI
Medos International Sàrl·10886705032303·
LEONE SPA
FDA UDI
LEONE SPA·08033707041047·DB BRACKETS 22 T-7 A+11 CUS U/L
Hongyun Powder-Free Vinyl Patient Examination Gloves, Clear( Non-colored)
FDA 510(k)
FDA Class 1
·General Hospital
SCORPIO NRG KNEE SYSTEM
FDA 510(k)
FDA Class 2
·Orthopedic
THERAPY ABLATION CATHETER
FDA Adverse Event
Malfunction
·IRVINE BIOMEDICAL, A ST. JUDE MEDICAL COMPANY·Product code OAD·June 25, 2010
ALARIS SYSTEM
FDA Adverse Event
Malfunction
·CAREFUSION SD·Product code FRN·November 2, 2023
MENTOR SILTEX ROUND MODERATE PROFILE
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FWM·November 28, 2018
PROXIMATE ILS CIRCULAR STAPLERS
FDA Adverse Event
Injury
·ETHICON ENDO-SURGERY, LLC.·Product code GDW·October 30, 2017
INFUSO.R.
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·September 10, 2011
GALILEO
FDA Adverse Event
Malfunction
·IMMUCOR, INC.·Product code KSZ·November 26, 2008
SYNCHROMED
FDA Adverse Event
Malfunction
·MEDTRONIC NEUROMODULATION·Product code LKK·July 23, 2013