12 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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GYRUS ACMI NEPHRO - EZDILATE NEPHROSTOMY BALLOON DILATION CATHETER
FDA 510(k)
FDA Unclassified
·Unknown
AGXO
FDA UDI
Oticon A/S·05707131258281·H160, RITE 312 WL CBE AGXO
FOSTER GILLIES NEEDLE HOLDER
FDA UDI
SONTEC INSTRUMENTS, INC.·00192896022249·FOSTER GILLIES NEEDLE HOLDER TUNGSTEN CARBIDE S...
Ophthalmic Spatula
FDA UDI
KATENA PRODUCTS, INC.·00841668102763·DODICK-KAMMANN CHOPPER ANGLED 1.5MM
MULTICLEAR MULTIWAVELENGTH TARGETED PHOTOTHERAPY SYSTEM
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
MICRODOT & MICRODOT XTRA
FDA 510(k)
FDA Class 2
·Clinical Chemistry
SIMPLYGO MINI
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CAW·November 17, 2023
DEXCOM G7 CONTINUOUS GLUCOSE MONITORING SYSTEM
FDA Adverse Event
Malfunction
·DEXCOM, INC.·Product code QBJ·May 29, 2025
SIMPLYGO MINI
FDA Adverse Event
Malfunction
·RESPIRONICS, INC.·Product code CAW·October 12, 2023
ONETOUCHPING GLUCOSEMGMTSYSTEM
FDA Adverse Event
Malfunction
·ANIMAS CORPORATION·Product code LZG·May 29, 2013
E SERIES DEFIBRILLATOR
FDA Adverse Event
Malfunction
·ZOLL MEDICAL CORPORATION·Product code MKJ·June 13, 2011
4 MOTOR ADVANCE BED
FDA Adverse Event
Malfunction
·HILL-ROM RITTER·Product code FNL·August 22, 2008