535 results
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23ms
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Sources: EU EUDAMED, US FDA
Filters
Regulation: Us FDA
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CAAS MR Solutions
FDA 510(k)
FDA Class 2
·Radiology
NA
FDA UDI
SYNTHES (U.S.A.) LP·10886982159700·3.5MM 90 DEG CANN LC-ANGLED BLADE PLATE 10 HOLE...
Introcan Safety ® 2
FDA UDI
B. BRAUN MEDICAL INC.·04046955341917·Introcan Safety 2 - 20G x 1.0 in., PUR, Winged
MEGA PLUS SPINE SYSTEM
FDA UDI
BK MEDITECH CO.,LTD.·08809665580351·Rod(CoCr), Ø5.5 x 70mm
GLOVETEX POWDER FREE LATEX EXAMINATION GLOVES, BLUE, NON-STERILE CONTAINS 50 MCGIN OR LESS OF TOTAL WATER EXTRACTABLE PR
FDA 510(k)
FDA Class 1
·General Hospital
STERICYCLE SHARPS MANAGEMENT SERVICE REUSABLE SHARPS CONTAINER, 2 GALLON, RED, STERICYCLE SHARPS MANAGEMENT SERVICES REU
FDA 510(k)
FDA Class 2
·General Hospital
Cable-Ready®
FDA UDI
Zimmer, Inc.·00889024039568·
Cable-Ready®
FDA UDI
Zimmer, Inc.·00889024039551·
INRATIO
FDA Adverse Event
Malfunction
·HEMOSENSE, INC.·Product code JPA·February 28, 2007
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC / HUNTINGTON·Product code HQL·June 21, 2007
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·November 6, 2007
ACRYSOF RESTOR
FDA Adverse Event
Other
·ALCON LABORATORIES, INC./HUNTINGTON·Product code HQL·November 6, 2007
BIOLOX PROSTHESIS HEAD 12/14 32MM S
FDA Adverse Event
Malfunction
·AESCULAP IMPLANT SYSTEMS·Product code LWJ·July 23, 2016
ENDO STITCH SURGIDAC 0 48 GRN DLU SU
FDA Adverse Event
Malfunction
·NORTH HAVEN - USS·Product code MFJ·May 23, 2007
LIFEPAK 20 DEFIBRILLATOR / MONITOR
FDA Adverse Event
Other
·MEDTRONIC EMERGENCY RESPONSE SYSTEMS·Product code LDD·April 26, 2007
SURGIPRO* 3 X 5 MONOFILAMENT MESH
FDA Adverse Event
Injury
·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code FTL·November 6, 2014
INFUSOR
FDA Adverse Event
Malfunction
·BAXTER HEALTHCARE - IRVINE·Product code MEB·September 1, 2011
SELUTE PICOTIP
FDA Adverse Event
Injury
·CPI - DEL CARIBE·Product code NVN·July 17, 2013
MALLINCKRODT
FDA Adverse Event
Injury
·JUAREZ HENEQUEN·Product code BSR·January 23, 2007
ENDOPATH XCEL DILATING TIP TROCAR WITH STABILITY SLEEVE - 12 MM DIAMETER, 100 MM
FDA Adverse Event
Malfunction
·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code GCJ·October 24, 2007