11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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COILS, MODELS MCF-B65, MCF-75, MCF-125 AND COOL-B65
FDA 510(k)
FDA Class 2
·Neurology
Nasal Speculum
FDA UDI
KATENA PRODUCTS, INC.·00841668108543·NASAL SPECULUM CHILD
Australis ALIF Cage
FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215127985·
MODIFICATION TO THE I.C.O.S SCREW
FDA 510(k)
FDA Class 2
·Orthopedic
MODIFICATION TO COOK ZILVER BILIARY STENT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
CONSULTA CRT-D
FDA Adverse Event
Injury
·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code NIK·April 22, 2013
UNKNOWN PAINPUMP PRODUCT
FDA Adverse Event
Injury
·STRYKER INSTRUMENTS KALAMAZOO·Product code FRN·April 21, 2011
HEARTSTREAM XL
FDA Adverse Event
Malfunction
·AGILENT TECHNOLOGIES INC.·Product code MKJ·July 8, 2008
BD VACUTAINER® 9NC 0.129M PLUS BLOOD COLLECTION TUBES
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·December 19, 2018
BELIFU
FDA Adverse Event
Injury
·HONG QIANGXING (SHEN ZHEN) ELECTRONICS LIMITED·Product code GZJ·February 10, 2020
BD VACUTAINER® PLUS PLASTIC CITRATE TUBE
FDA Adverse Event
Malfunction
·BECTON, DICKINSON AND COMPANY (BD)·Product code JKA·August 7, 2018