28 results · 22ms · Sources: EU EUDAMED, US FDA

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Weck Auto Endo5 Hem-o-lok Ligating Clip Applier

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

NA

FDA UDI
Gc America Inc.·10386040012393·PLUNGER FOR UNIVERSAL DISPENSER

NA

FDA UDI
Gc America Inc.·D6581520811·PLUNGER FOR UNIVERSAL DISPENSER

Staple Sizer - Orange

FDA UDI
SIGNATURE ORTHOPAEDICS PTY LTD·09348215165253·

ENDOSCOPIC CLIP SYSTEM

FDA 510(k)
FDA Class 2 ·General, Plastic Surgery

REMOTE ACCESS PERFUSION (RAP) FEMORAL VENOUS CANNULA

FDA 510(k)
FDA Class 2 ·Cardiovascular

IDENTITY ADX XL DR

FDA Adverse Event
Malfunction ·ST. JUDE MEDICAL, INC., CARDIAC RHYTHM MANAGEMENT DIVISI·Product code DXY·January 13, 2014

PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

FDA Adverse Event
Injury ·AV-TEMECULA-CT·Product code MGB·July 7, 2011

PELVICOL ACELLULAR COLLAGEN MATRIX

FDA Adverse Event
Injury ·TISSUE SCIENCE LABORATORIES·Product code FTL·May 29, 2013

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 30, 2022

OHICHO3

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·March 18, 2026

BD POSIFLUSH¿ NORMAL SALINE SYRINGES

FDA Adverse Event
Malfunction ·BD MEDICAL (BD WEST) MEDICAL SURGICAL·Product code NGT·March 31, 2022

METACROSS OTW PTA BALLOON DILATATION CATHETER

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 19, 2019

OHICHO NEO

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·February 7, 2024

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·December 26, 2019

SHIRANUI EX

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

OHICHO3

FDA Adverse Event
Injury ·Product code LIT·July 19, 2019

ProScreen CLIA Waived Cup 6 Drugs w/Adul, Item No. PSCupA-6MB-W

FDA Enforcement
Class III ·Terminated·Ameditech Inc·December 30, 2015

PTA BALLOON CATHETER(OHICHO3)

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·December 13, 2017

SHIRANUI EX

FDA Adverse Event
Injury ·KANEKA CORPORATION·Product code LIT·August 14, 2020