27 results
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21ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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Needle aspiration and injection
FDA UDI
KATENA PRODUCTS, INC.·00841668113615·PERIBULBAR NEEDLE 23GA 32MM
Spectral CT
FDA 510(k)
FDA Class 2
·Radiology
Elite HD+ Regular Body Normal Set
FDA UDI
ZHERMACK SPA·EZHIC2030201·Addition silicone impression material
KARL STORZ MODEL 203020 20 EQUIMAT
FDA 510(k)
FDA Class 2
·Gastroenterology, Urology
KARL STORZ MODEL 203020 20 EQUIMAT
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
CARDIAC FUNCTION LABORATORY; PRESSURE INTERFACE; PRESSURE / VOLUME CATHETER
FDA 510(k)
FDA Class 2
·Cardiovascular
AGFA MAMORAY MAMMOGRAPHIC CASSETTE, AGFA METAL-BODIED CAWO CASSETTE, AGFA CURIX AND LIGHTWEIGHT CASSETTE
FDA 510(k)
FDA Class 2
·Radiology
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080737·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024578739·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080744·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024578760·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024578746·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080751·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024080720·
XtraFix®
FDA UDI
Zimmer, Inc.·00889024578753·
TRIPOD HEART STABILIZER - NYLON FASTRACT
FDA Adverse Event
Malfunction
·CHASE MEDICAL·Product code MWS·October 2, 2013
9800
FDA Adverse Event
Malfunction
·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 18, 2014
ATTAIN OTW
FDA Adverse Event
Malfunction
·MEDTRONIC, INC.·Product code DTB·August 11, 2011
SYNCHROMED EL
FDA Adverse Event
Malfunction
·MEDTRONIC·Product code LKK·July 2, 2013
Stryker brand OrthoTec pulsed irrigation/suction handpiece and tubing set; part number 0203-020-000.
FDA Recall
Terminated
·Stryker Instruments, Instruments Div.·Product code FPK·November 12, 2003