53 results · 33ms · Sources: EU EUDAMED, US FDA

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Cryotop Vitrification Kit and Cryotop Thawing Kit

FDA 510(k)
FDA Class 2 ·Obstetrics/Gynecology

N/A

FDA UDI
GEORGE TIEMANN & CO.·B5821608640·CLAMP, SURGICAL, GENERAL & PLASTIC SURGERY

MULTIDIRECTIONAL THREADED PEG

FDA 510(k)
FDA Class 2 ·Orthopedic

BIOSPINE VBR SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BD VERITOR¿ SYSTEM FOR RAPID DETECTION OF FLU A+B LABORATORY KIT

FDA Adverse Event
Malfunction ·BD RAPIS DIAGNOSTICS (SUZHOU) CO. LTD.·Product code PSZ·March 3, 2026

CARELINK

FDA Adverse Event
Malfunction ·MEDTRONIC, INC.·Product code KRG·October 10, 2014

OT VERIO IQ METER

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

PROMUS EVEROLIMUS ELUTING CORONARY STENT SYSTEM

FDA Adverse Event
Malfunction ·AV-TEMECULA-CT·Product code NIQ·July 13, 2011

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·May 7, 2018

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017

BIODESIGN DURAL GRAFT

FDA Adverse Event
Injury ·COOK BIOTECH·Product code GXQ·December 4, 2017