86 results
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31ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HIVOX SELF ADHESIVE ELECTRODE GEL PADS
FDA 510(k)
FDA Class 2
·Neurology
Bernafon
FDA UDI
Bernafon AG·05711584049761·PC7 N, PS SF DB PRECISO 7
Young
FDA UDI
YOUNG DENTAL MANUFACTURING I, LLC·00302731317205·Young DPA Classic, Latex Free, Firm, Long, Blue...
NC Screw-retained Abutment
FDA UDI
BIO CONCEPT Co., Ltd.·06947600381136·
Pro-Link Ti
FDA UDI
Life Spine, Inc.·00190837081072·
Medetz Surgical Instruments
FDA UDI
Medetz Surgical Instruments LLC·G2231317200·Iris Scissors 4 1/2" curved
TALOS® IBF
FDA UDI
MEDITECH SPINE, LLC·B167311317200·
TALOS® HA PEEK IBF
FDA UDI
MEDITECH SPINE, LLC·B167321317200·
SOLITAIRE FR REVASCULARIZATION DEVICE
FDA Adverse Event
Injury
·COVIDIEN (IRVINE)·Product code NRY·August 25, 2015
MODIFICATION TO HERMES O.R. CONTROL CENTER
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
JULIET OL
FDA 510(k)
FDA Class 2
·Orthopedic
EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE
FDA Adverse Event
Malfunction
·AIZU OLYMPUS CO., LTD.·Product code FDS·July 22, 2022
SCRDRIVERSHAFT T25 F/URS
FDA Adverse Event
Malfunction
·SYNTHES GMBH·Product code HXX·May 29, 2013
ACUITY CATHETER
FDA Adverse Event
Injury
·EXTERNAL MANUFACTURER·Product code DQY·October 1, 2014
PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM
FDA Adverse Event
Injury
·AV-TEMECULA-CT·Product code MGB·June 16, 2011
audifon
FDA UDI
audifon GmbH & Co. KG·EADF030240980931317201·audifon risa R -- beige
RITE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF004656295531317201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF004032290931317201·BTE-TRT
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022197854231317201·RITE
audifon
FDA UDI
audifon GmbH & Co. KG·EADF022234855231317201·RITE-TRT