9,587 results
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38ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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ROOTT
FDA UDI
TRATE LLC·00810149980305·Implant driver, handpiece, S, R.
ROOTT
FDA UDI
TRATE LLC·00810149980411·Implant driver, handpiece, XS, R.
Diamatrix
FDA UDI
Diamatrix·00813059015167·Irrigating and Aspirating Handpiece Handle, 105...
Instrument Holder
FDA UDI
Taiwan Main Orthopaedic Biotechnology Co., Ltd.·04719878713733·
KPS-I, THE KIDNEY PERFUSION SOLUTION
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
Ozuufuk Tekstil Ith. Ihr. San. Ve Tic. Ltd. Sti
FDA registration
Ozuufuk Tekstil Ith. Ihr. San. Ve Tic. Ltd. Sti·1 product·🇹🇷 Türkiye
DORT-A TIP MALZ SAN ITH IHR TIC LTD STI
FDA registration
DORT-A TIP MALZ SAN ITH IHR TIC LTD STI·1 product·🇹🇷 Türkiye
PERSONAL TRANSPORT STRETCHER W ITH HEAD REST
FDA UDI
M.A.C. MEDICAL INC.·B286PT2000EYE1·PERSONAL TRANSPORT STRETCHER W ITH HEAD REST
PERSONAL TRANSPORT STRETCHER W ITH HEAD REST
FDA UDI
FUTURE HEALTH CONCEPTS, INC.·B337FHC7100EYE11·EYE MOBILE-CARE STRETCHER WITH CLEARLY MARKED H...
PERSONAL TRANSPORT STRETCHER W ITH HEAD REST
FDA UDI
M.A.C. MEDICAL INC.·B286FHC7100EYE11·EYE MOBILE-CARE STRETCHER WITH CLEARLY MARKED H...
PERSONAL TRANSPORT STRETCHER W ITH HEAD REST
FDA UDI
FUTURE HEALTH CONCEPTS, INC.·B337FHC7200EYE1·Mobilecare Stretcher; Standard Features Include...
PERSONAL TRANSPORT STRETCHER W ITH HEAD REST
FDA UDI
M.A.C. MEDICAL INC.·B286PT2000EYEWL1·PERSONAL TRANSPORT STRETCHER W ITH HEAD REST, W...
PERSONAL TRANSPORT STRETCHER W ITH HEAD REST, WRIST SHORT
FDA UDI
M.A.C. MEDICAL INC.·B286PT2000EYEWS1·PERSONAL TRANSPORT STRETCHER W ITH HEAD REST, W...
STERNAL ZIPFIX ITH NEEDLE STERILE
FDA Adverse Event
Injury
·SYNTEHS MONUMENT·Product code JDQ·May 16, 2012
ANEURX STENT GRAFT (HDM FLEXIBLE) ITH XPEDIENT
FDA Adverse Event
Injury
·MEDTRONIC VASCULAR·Product code MIH·February 1, 2005
PROGAV 2.0 SYS W/ITH SA10 A.CONTROL RESERVOIR
FDA Adverse Event
Injury
·CHRISTOPH MIETHKE GMBH & CO KG·Product code JXG·January 13, 2025
ELECSYS 2010 RACK
FDA Adverse Event
Malfunction
·ROCHE DIAGNOSTICS·Product code MMI·February 6, 2009
Spectralis HRA + OCT and variants (e.g.s below), Spectralis FA+OCT, Spectralis ICGA+OCT, Spectralis OCT Blue Peak, Spectralis OCT ith Multicolor
FDA 510(k)
FDA Class 2
·Ophthalmic
STYLE 168 SALINE FILLED BREAST IMPLANT
FDA Adverse Event
Injury
·ALLERGAN (COSTA RICA)·Product code FWM·August 27, 2024
LAP-BAND ADJUSTABLE GASTRIC BANDING SYSTEM
FDA Adverse Event
Malfunction
·BIOENTERICS CORPORATION·Product code LTI·September 14, 2004