27 results · 33ms · Sources: EU EUDAMED, 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