12 results
·
20ms
·
Sources: EU EUDAMED, US FDA
RAIN-X
FDA 510(k)
FDA Class 1
·Anesthesiology
Gen. Acces/ Instr. Tip Guard
FDA UDI
KATENA PRODUCTS, INC.·00841668112311·SURG-I-BAND BLUE
Continuum® Trilogy®
FDA UDI
Zimmer, Inc.·00889024152601·
VESOCCLUDE LIGATING CLIP
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ACIST CVI1 Contrast Delivery System, A1000 Syringe Kit, A1000V Syringe Kit, BT2000 Manifold Kit, BT2000 Manifold Kit, AngioToiuch Hand Controller Kit
FDA 510(k)
FDA Class 2
·Cardiovascular
NA
FDA UDI
Zimmer, Inc.·00889024192898·
N/A
FDA UDI
Zimmer, Inc.·00889024192881·
N/A
FDA UDI
Zimmer, Inc.·00889024192874·
N/A
FDA UDI
Zimmer, Inc.·00889024192867·
UNIFY ASSURA CRT-D
FDA Adverse Event
Malfunction
·ST. JUDE MEDICAL, INC., CRMD·Product code NIK·May 5, 2014
CAPSUREFIX NOVUS
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012
SPRINT QUATTRO SECURE
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO, INC.·Product code LWS·August 10, 2010