11 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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Helios+ UV-C System
FDA 510(k)
FDA Class 2
·General Hospital
NA
FDA UDI
Richard Wolf GmbH·04055207014653·PARENCHYM CLAMP Ø 5MM WL 280MM by Linder, jaw ...
Richard-Allan® Needle 1/2 Circle Trocar
FDA UDI
ASPEN SURGICAL PRODUCTS, INC.·00840113217991·Intent to be used with suture material for tiss...
ABSORBENT PAPER POINTS
FDA UDI
DiaDent Group International·08806383516181·"An absorbent paper points is an endodontic pap...
Symbia VA10A Family
FDA 510(k)
FDA Class 2
·Radiology
VALLY FORGE SCIENTIFIC MALIS BIPOLAR DISPOSABLE FINGER OPERATED ELECTROSURGICAL INSTRUMENTS
FDA 510(k)
FDA Class 2
·General, Plastic Surgery
SPECIAL EVD 10-110 W/O Y SITE
FDA Adverse Event
Malfunction
·INTEGRA NEUROSCIENCES PR·Product code JXG·July 15, 2020
PINN MAR NEUT 28IDX52OD
FDA Adverse Event
Injury
·DEPUY ORTHOPAEDICS, INC.·Product code LPH·November 20, 2008
DURATA STS OPTIM ACTIVE FIXATION, DF-4 CONNECTOR
FDA Adverse Event
Injury
·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NVY·September 10, 2011
GYNECARE TVT RETROPUBIC SYSTEM
FDA Adverse Event
Injury
·ETHICON INC.·Product code OTN·July 23, 2013
2) Signa Advantage SP (K942604 Signa Advantage SP MR System) A magnetic resonance diagnostic device is intended for general diagnostic use to present images which reflect the spatial distribution and/or magnetic resonance spectra which reflect frequency and distribution of nuclei exhibiting nuclear magnetic resonance. Other physical parameters derived from the images and/or spectra may also be produced. The device includes hydrogen-1 (proton) imaging, sodium-23 imaging, hydrogen-1 spectroscopy, phosphorus-31 spectroscopy, and chemical shift imaging (preserving simultaneous frequency and spatial information).
FDA Recall
Terminated
·GE Healthcare, LLC·Product code LNH·November 9, 2010