15 results
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20ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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DUAL LUMEN CATHETER, MODEL DL-35-90
FDA 510(k)
FDA Class 2
·Cardiovascular
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79916011·Sprint II Bracket McLaugh/Benn/Trev. .022" mand...
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79916011001·Sprint II Bracket McLaugh/Benn/Trev. .022" mand...
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79916010101·Sprint II Bracket McLaugh/Benn/Trev. .022" mand...
Sprint®
FDA UDI
Forestadent Bernhard Förster GmbH·EFOR79916010051·Sprint II Bracket McLaugh/Benn/Trev. .022" mand...
BA 1/2 KIT,BE,P37,INL,1',STKR
FDA UDI
CURBELL MEDICAL PRODUCTS, INC.·00840828136761·BA 1/2 KIT,BE,P37,INL,1',STKR
CD 3700 SL
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·May 23, 2007
Valleylab FT10 Electrosurgical Platform
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
ELECYS ANTI-CCP CALCHECK
FDA 510(k)
FDA Class 1
·Clinical Chemistry
HDI 5000 ULTRASOUND STANDARD SYSTEM
FDA Adverse Event
Malfunction
·PHILIPS ULTRASOUND, INC.·Product code IYO·March 30, 2012
CELL-DYN 3700 SL ANALYZER
FDA Adverse Event
Malfunction
·ABBOTT DIAGNOSTICS DIVISION·Product code GKZ·February 22, 2019
PRIMEADVANCED
FDA Adverse Event
Malfunction
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·March 6, 2013
CARELINK
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code KRG·August 8, 2014
ATTAIN OTW
FDA Adverse Event
Injury
·MEDTRONIC PUERTO RICO, INC.·Product code DTB·February 15, 2011
TI MATRIX LOCKING CAP
FDA Adverse Event
Malfunction
·SYNTHES BRANDYWINE·Product code NKB·July 23, 2015