425 results · 30ms · Sources: EU EUDAMED, US FDA

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V.A.C. ABDOMINAL DRESSING

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

Safco polycarbonate crowns

FDA UDI
SAFCO DENTAL SUPPLY CO.·D72310220113·Safco polycar crwn up/low ant 150crwn

EVOS Lumbar Interbody System

FDA UDI
Cutting Edge Spine, LLC·00841193107103·HA PEEK EVOS Straight, ,11mmx9mmx 22mm , BICONV...

OsteoMed

FDA UDI
OSTEOMED LLC·00845694018586·2.0mm x 11mm Lag Screw

OsteoMed

FDA UDI
OSTEOMED LLC·00845694066464·HPS 2.0 x 11mm Lag Screw Sterile Qty 5

MODIFICATION TO A620 EEG

FDA 510(k)
FDA Class 2 ·Neurology

GLUTARTEST 1 REAGENT STRIP

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

AUTOPULSE NIMH BATTERY

FDA Adverse Event
ZOLL CIRCULATION, INC.·Product code DRM·January 29, 2013

TGS UKA FEMORAL AND TIBIAL COMPONENTS

FDA Adverse Event
Injury ·ALEXANDRIA RESEARCH TECHNOLOGIES, INC.·Product code HSX·March 21, 2012

CONSERVE(R) TOTAL A-CLASS HEAD

FDA Adverse Event
Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code JDL·July 26, 2011

HEARTSTREAM FR2

FDA Adverse Event
Malfunction ·PHILIPS MEDICAL SYSTEMS (HTST)·Product code MKJ·December 12, 2011

MEDGYN FLEXIBLE CURETTE 11MM REF. NO. 022011

FDA Adverse Event
Malfunction ·MEDGYN PRODUCTS, INC.·Product code HCY·April 15, 2005

DIAGNOST 97 - MCP/SCP - DSI

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE·Product code JAA·February 1, 2011

IMPLANTABLE CARDIOVERTER DEFIBRILLATOR (NON-CRT)

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code LWS·August 11, 2023

PARADIGM REAL-TIME INSULIN INFUSION PUMP

FDA Adverse Event
Injury ·MEDTRONIC MINIMED·Product code OYC·March 26, 2013

CARDIOVASCULAR PROCEDURE KIT

FDA Adverse Event
Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORPORATION·Product code OEZ·March 10, 2011

ESSIX C+ PLASTIC MATERIAL

FDA Adverse Event
Injury ·DENTSPLY RAINTREE ESSIX·Product code MQC·March 31, 2008

CESAR/C-STANDFLOOR-OMCP-VISUB-CCD(V5000)

FDA Adverse Event
Malfunction ·PHILIPS HEALTHCARE·Product code IZI·February 1, 2011

ACCU-CHEK COMPACT TEST DRUM

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·January 5, 2010

MEDTRONIC

FDA Adverse Event
Malfunction ·MEDTRONIC·Product code DTB·August 12, 2023