10 results
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19ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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LARGE VOLUME ELASTOMERIC INFUSION DEVICE ATTACH.
FDA 510(k)
FDA Class 2
·General Hospital
REVELATION DIAMOND
FDA UDI
Ss White Burs, Inc.·D6909104252·REVELATION DIAMOND 880-021C - 5 PACK
DeRoyal
FDA UDI
DEROYAL INDUSTRIES, INC.·00749756352079·DR DILLIN SHOULDER PACK
Kalitec Universal Instruments
FDA UDI
Kalitec Direct LLC·B07301K1104250·Tray, Base, 4.25", Arcamed
NIDO Pedicle Screw System
FDA UDI
Kalitec Direct LLC·B07315K1104250·Tray, 4.25 Inch Base
HC-BIOS DENTAL IMPLANT
FDA 510(k)
FDA Class 2
·Dental
EPIDURAL CATHETER WITH CONNECTOR (AND ACCESSORY)
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
REJUVENATE MODULAR NECK
FDA Adverse Event
Injury
·STRYKER ORHTOPAEDICS CORK·Product code MEH·January 8, 2013
AVAULTA PLUS BIOSYNTHETIC SUPPORT SYSTEM
FDA Adverse Event
Injury
·C.R. BARD, INC.·Product code FTL·November 18, 2010
PATELLA CLAMP
FDA Adverse Event
Malfunction
·STRYKER ORTHOPAEDICS-MAHWAH·Product code JWH·July 2, 2014