27 results
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33ms
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Sources: EU EUDAMED, US FDA
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Regulation: Us FDA
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HARALD NORDIN GLASSIX GLASS FIBER COMPOSITE DENTAL POST
FDA 510(k)
FDA Class 1
·Dental
Custom Procedure Kit
FDA UDI
MEDIVATORS INC.·40677964022607·The ENDO CARRY-ON Procedure Kit contains all of...
DermaCol 100 Sheet
FDA UDI
Sion Brands LLC·00714196391353·
DermaCol 100 Sheet
FDA UDI
Sion Brands LLC·00714196033215·
Alpha-Tec Systems
FDA UDI
Alpha-TEC Systems, Inc.·00816085020426·CELL-BOND Slides, 2 Wells, black background
Localite TMS Navigator TS
FDA UDI
LOCALITE GmbH·G076A003221A0·
NA
FDA UDI
STRYKER CORPORATION·04546540466587·Precision Thin w/12.0mm Stop (9.0 x 0.38 x 25.0mm)
SERIES 7700 MOBILE C-ARM, COMPACT 7700 MOBILE C-ARM, COMPACT 7700 PLUS MOBILE C-ARM
FDA 510(k)
FDA Class 2
·Radiology
MALE LATEX COMDOM WITH DOTTED SURFACE
FDA 510(k)
FDA Class 2
·Obstetrics/Gynecology
BD DISCARDIT¿ II SYRINGE
FDA Adverse Event
Malfunction
·BECTON DICKINSON, S.A.·Product code FMF·August 25, 2021
SCREW, FIXATION, BONE
FDA Adverse Event
Malfunction
·ACUMED LLC·Product code HWC·December 18, 2017
SMALL BATTERY DRIVE
FDA Adverse Event
Malfunction
·SYNTHES OBERDORF·Product code HWE·March 13, 2014
OT VERIO IQ METER
FDA Adverse Event
Malfunction
·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·March 14, 2013
TRANSTAR STRETCHER
FDA Adverse Event
Malfunction
·HILL-ROM, INC.·Product code FNL·February 22, 2011
ACCU-CHEK ULTRAFLEX INFUSION SET
FDA Adverse Event
Malfunction
·DISETRONIC MEDICAL SYSTEMS·Product code FPA·February 21, 2008
Z.S.G.M. CUTTER 3:1 RATIO ( CAUTION: SHARP )
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·August 2, 2023
Z.S.G.M. CUTTER 1.5:1 RATIO ( CAUTION: SHARP )
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·August 2, 2023
Z.S.G.M. CUTTER 4:1 RATIO ( CAUTION: SHARP )
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·August 2, 2023
Z.S.G.M. CUTTER 2:1 RATIO ( CAUTION: SHARP )
FDA Adverse Event
Malfunction
·ZIMMER SURGICAL, INC.·Product code FZW·August 2, 2023
BIO-CORKSCREW SUTURE ANCHOR
FDA Adverse Event
Injury
·ARTHREX, INC.·Product code MAI·February 21, 2007