13 results
·
19ms
·
Sources: EU EUDAMED, US FDA
RITE-BITE BIOPSY FORCEPS
FDA 510(k)
FDA Class 2
·Ear, Nose, Throat
P.F.C. SIGMA
FDA UDI
DEPUY (IRELAND)·10603295230465·P.F.C. SIGMA TIBIAL INSERT ROTATING PLATFORM RP...
AuST Steerable Sheath
FDA 510(k)
FDA Class 2
·Cardiovascular
Universa Soft Ureteral Stents and Stent Sets
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
COBE SPECTRA BLOOD COLLECTION
FDA Adverse Event
TERUMO BCT·Product code GKT·February 8, 2013
VITALITY 2
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code KRG·July 22, 2014
TELIGEN
FDA Adverse Event
Malfunction
·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 6, 2011
IMPELLA CP
FDA Adverse Event
Injury
·ABIOMED, INC.·Product code OZD·December 8, 2025
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·January 29, 2019
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Malfunction
·COOK UROLOGICAL INC·Product code FAD·May 13, 2016
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Injury
·COOK INC·Product code FAD·September 8, 2016
UNIVERSA SOFT URETERAL STENT SET
FDA Adverse Event
Injury
·COOK UROLOGICAL INC·Product code FAD·May 13, 2016
UNKNOWN
FDA Adverse Event
Malfunction
·COOK INC·Product code FAD·July 23, 2019