9 results
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24ms
·
Sources: EU EUDAMED, US FDA
MED-TEC HAND GRIP
FDA 510(k)
FDA Class 2
·Radiology
BASE
FDA UDI
Nuvasive, Inc.·00887517701466·BASE HL Trial, 12x34x24mm 25°
P.F.C. SIGMA
FDA UDI
DEPUY INTERNATIONAL LTD·10603295231257·P.F.C. SIGMA TRIAL FEMORAL COMPONENT - RPF SIZE...
BOSS Instruments
FDA UDI
BOSS INSTRUMENTS, LTD., INC.·00888515246966·Colver Tonsil Knfe/Diss, 8 1/4"
ALLERGAN I.S.P. MODEL 3000 OPHTHALMIC SURGICAL-SYS
FDA 510(k)
FDA Class 2
·Ophthalmic
Arm Blood Pressure Monitor (HH-802CB, HH-802EB, HH-805CB, HH-812CB, HH-808CL, HH-808EL)
FDA 510(k)
FDA Class 2
·Cardiovascular
OBTAPE TRANSOBTURATOR SLING
FDA Adverse Event
Injury
·MENTOR WORLDWIDE LLC·Product code FTL·February 7, 2013
COGNIS
FDA Adverse Event
Injury
·GUIDANT CRM CLONMEL IRELAND·Product code NIK·January 10, 2011
THERMOCOOL® SMARTTOUCH® UNI-DIRECTIONAL NAVIGATION CATHETER
FDA Adverse Event
Malfunction
·BIOSENSE WEBSTER, INC. (JUAREZ)·Product code LPB·July 24, 2014