41 results · 25ms · Sources: EU EUDAMED, US FDA

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INTRAFIX(TM) Advance Tibial Fastener System

FDA 510(k)
FDA Class 2 ·Orthopedic

MEDI

FDA UDI
MEDI MANUFACTURING, INC.·04051526159853·PROTECT.ACHI ANKLE SUPPORT GRAY IV

Cardiovascular Procedure Kit

FDA UDI
Terumo Cardiovascular Systems Corporation·00699753499768·

AMT G-J TUBE

FDA 510(k)
FDA Class 2 ·Gastroenterology, Urology

COLLAGRAN-COLLAGEN WOUND DRESSING, COLLAGRANAG-COLLAGEN W/SILVER ANTIMICROBIAL WOUND DRESSING

FDA 510(k)
FDA Unclassified ·Unknown

ATLAS II PLUS DR

FDA Adverse Event
Injury ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code LWS·January 13, 2014

COLLEAGUE PRE P1.7

FDA Adverse Event
Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·July 13, 2011

OT VERIO IQ METER

FDA Adverse Event
Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2013

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·September 11, 2022

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·April 14, 2026

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 24, 2021

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·January 11, 2022

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·January 29, 2026

SHIRANUI HP

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·May 18, 2020

PRODIGY AUTOCODE

FDA Adverse Event
Injury ·OK BIOTECH CO., LTD.·Product code NBW·April 9, 2020

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·October 22, 2024

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 12, 2020

CXI SUPPORT CATHETER

FDA Adverse Event
Injury ·COOK INC·Product code KRA·April 18, 2019

SHIRANUI HP

FDA Adverse Event
Malfunction ·KANEKA CORPORATION·Product code LIT·April 24, 2019

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·December 6, 2024