12 results
·
29ms
·
Sources: EU EUDAMED, US FDA
HUGHES BLADDER AND BOWEL TRAINING SYSTEM(AD-T-18, MED-18,MED-1,MED-T-1,MEDD-18,MED-38,MED-T-10,MED-T-25,MED-T-5
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
PEEK Corpectomy
FDA UDI
Nuvasive, Inc.·00887517623973·PEEK Corp Core, Ø14x42mm
Exofin Fusion Skin Closure System
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SUPRASORB A +AG
FDA 510(k)
FDA Unclassified
·Unknown
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·April 30, 2026
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·December 3, 2025
BD VACUTAINER® K2 EDTA (K2E) 10.8 MG BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON & CO.·Product code JKA·May 22, 2018
FISHER & PAYKEL HEALTHCARE
FDA Adverse Event
Malfunction
·FISHER & PAYKEL HEALTHCARE LTD·Product code FMT·October 16, 2025
LOGIC CR TIB INSERT STD, SZ 5, 9MM
FDA Adverse Event
Injury
·EXACTECH, INC.·Product code JWH·June 4, 2024
POWERED WHEELCHAIR
FDA Adverse Event
INVACARE REHABILITATION EQUIP·Product code ITI·July 31, 2014
PRECISION XTRA
FDA Adverse Event
Malfunction
·Product code NBW·January 27, 2011
PULMONETIC
FDA Adverse Event
Malfunction
·PULMONETIC SYSTEMS, INC.·Product code CBK·October 4, 2007