11 results
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22ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Passport Series Patient Monitors(Passport 12m, Passport 17m)
FDA 510(k)
FDA Class 2
·Cardiovascular
Millennium
FDA UDI
Avalign Technologies, Inc.·00190776177621·BREISKY .
COMFORT TOUCH INSUIN PEN NEEDLES
FDA Adverse Event
Malfunction
·JIANGSU CAINA TECHNOLOGY CO., LTD.·Product code FMI·May 21, 2021
STRYKER TWIST DRILLS
FDA 510(k)
FDA Class 2
·Neurology
AESCULAP MONOMAX ABSORBABLE SUTURE
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
HEARTSTART MRX
FDA Adverse Event
Malfunction
·PHILIPS MEDICAL SYSTEMS·Product code MKJ·June 5, 2013
ACCU-CHEK SPIRIT
FDA Adverse Event
Malfunction
·ROCHE INSULIN DELIVERY SYSTEMS, INC.·Product code LZG·June 22, 2011
PARADIGM REAL-TIME INSULIN INFUSION PUMP
FDA Adverse Event
Malfunction
·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·October 14, 2014
QUADRA-H CEMENTLESS, HA COATED STD STEM SIZE 7
FDA Adverse Event
Injury
·MEDACTA INTERNATIONAL SA·Product code JDI·March 5, 2021
MONOMAX VIOLET 1(4)150CM HRT48 LOOP(M
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code NWJ·June 4, 2019
MONOMAX VIOLET 1(4)150CM HRT48 LOOP(M
FDA Adverse Event
Malfunction
·B.BRAUN SURGICAL SA·Product code NWJ·June 4, 2019