13 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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IU Implant System
FDA 510(k)
FDA Class 2
·Dental
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00763000878399·TRIAL 2172345 O25 IB 20MM 12 DEG 12X45
PIVOX™ Oblique Lateral Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00643169595422·TRIAL 2172345 O25 IB 20MM 12 DEG 12X45
ATRAMAT
FDA UDI
Internacional Farmacéutica, S.A. de C.V.·07500142063756·ATRAMAT SILK SURGICAL SUTURE BLACK USP 3-0 EP 2...
UniTip High Resolution Catheter
FDA UDI
Unisensor AG·07640172970508·
EASYMAX T1 SELF MONITORING BLOOD GLUCOSE SYSTEM, MODEL EPS10042
FDA 510(k)
FDA Class 2
·Clinical Chemistry
POWRSYRINGE MONITOR
FDA 510(k)
FDA Class 2
·General Hospital
GMK-HINGE FEMORAL COMPONENT SIZE 3 R
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code KRO·July 25, 2022
INTERSTIM
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·June 23, 2011
TRILOGY 100
FDA Adverse Event
Malfunction
·RESPIRONICS INC.·Product code CBK·June 5, 2013
BIRD
FDA Adverse Event
Malfunction
·CARDINAL HEALTH 207, INC.·Product code BZR·September 19, 2008
UNITIP CATHETER FOR HR GI
FDA Adverse Event
Malfunction
·UNISENSOR USA INC·Product code FFX·January 16, 2015
BAIR HUGGER / 3M
FDA Adverse Event
Injury
·3M·Product code DWJ·November 23, 2016