11 results
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20ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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MATRX BATTERY CHARGER/DEFIBRILLATOR TESTER
FDA 510(k)
FDA Class 2
·Cardiovascular
Precept
FDA UDI
Nuvasive, Inc.·00887517386717·PRECEPT Screw Shank, 5.5x25mm Modular
CD HORIZON® Spinal System
FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994291592·SCREW 7895525 CDH PEEK 5.5X25 NON CANN
MEGA PLUS MIS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809916497100·Long-arm Multi-Axial Fenestrated Screw, Ø5.5 x ...
M-46 GOLD BASE DENTAL ALLOY
FDA 510(k)
FDA Class 2
·Dental
INTERTON BTE HEAR AID, SUPRA, SUPREMA, MINETTA
FDA 510(k)
FDA Class 1
·Ear, Nose, Throat
HOMECHOICE AUTOMATED PD SET WITH CASSETTE
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·June 25, 2014
MARYLAND BIPOLAR FORCEPS INSTRUMENT
FDA Adverse Event
Malfunction
·INTUITIVE SURGICAL,INC.·Product code NAY·January 3, 2013
COLLEAGUE CXE1 PUMP UNREFURB
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·November 10, 2010
PERCUTANEOUS TRAY
FDA Adverse Event
Malfunction
·DEROYAL INDUSTRIES, INC.·Product code OEQ·October 22, 2018
NCIRCLE TIPLESS STONE EXTRACTOR
FDA Adverse Event
Malfunction
·COOK INC·Product code FFL·July 21, 2017