9 results
·
19ms
·
Sources: EU EUDAMED, US FDA
INNOVATIONS NASAL TAMPON
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756665643·EXTREMITY TRAY II-CANDLER HOSP
BEHIND-THE-EAR HEARING AID MODEL 304 PP-AGC-I
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
SURGICAL RETRACTORS
FDA 510(k)
FDA Class 1
·General, Plastic Surgery
NXSTAGE SYSTEM ONE
FDA Adverse Event
Injury
·NXSTAGE MEDICAL, INC.·Product code KDI·June 16, 2014
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·July 7, 2015
TENDRIL ST
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·November 10, 2010
MENTOR MEMORYSHAPE¿ MH 555CC
FDA Adverse Event
Injury
·MENTOR TEXAS·Product code FTR·June 4, 2024
Latex-free, Primary I.V. Set, vented, 73 inch with flashback bulb, 15 drops/mL, a sterile Rx single use device, Hospira Inc, Lake Forest, IL USA. Made in Costa Rica, list 8962-48.
FDA Recall
Terminated
·Hospira Inc.·Product code FPA·November 24, 2009