24 results · 24ms · Sources: EU EUDAMED, US FDA

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OXFORD ANKLE FUSION NAIL(AFN) SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

RZ Medizintechnik GmbH

FDA UDI
RZ-Medizintechnik GmbH·04049197041195·Super-Cut Aufricht Scissors curved...

OBC-127 BREAST ARRAY COIL

FDA 510(k)
FDA Class 2 ·Radiology

APEX MODULAR HEAD, SIZE 28 ,32, 26 AND 40 MM+10.5 OFFSET, MODELS 302810, 303210,303610,304010

FDA 510(k)
FDA Class 2 ·Orthopedic

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·August 5, 2019

OMNIPOD 5 POD

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code QFG·June 1, 2023

OMNIPOD DASH INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·October 3, 2023

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·September 6, 2019

OMNIPOD DASH INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Death ·INSULET CORPORATION·Product code LZG·July 19, 2023

ASPHERE M SPEC 12/14 36 +5

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS INC US·Product code KWA·May 21, 2013

OPTIFLUX 160NRE DIALYZER FINISHED ASSY.

FDA Adverse Event
Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code FJI·July 29, 2014

ASR UNI FEMORAL IMPL SIZE 43

FDA Adverse Event
Injury ·DEPUY INTERNATIONAL, LTD.·Product code KWA·June 2, 2011

EQUINOXE

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·February 5, 2019

OMNIPOD DASH INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·December 13, 2023

OMNIPOD DASH, PODS 10-PACK

FDA Adverse Event
Malfunction ·INSULET CORPORATION·Product code LZG·May 9, 2023

SPECIFIC DEVICE NOT REPORTED

FDA Adverse Event
Injury ·EXACTECH, INC.·Product code KWT·July 7, 2025

OMNIPOD INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Injury ·INSULET CORPORATION·Product code LZG·January 23, 2024

OMNIPOD DASH¿ INSULIN MANAGEMENT SYSTEM

FDA Adverse Event
Injury ·INSULET CORPORATION·Product code LZG·July 21, 2022

BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 2, 2019

BD VACUTAINER® K2 EDTA (K2E) 7.2MG BLOOD COLLECTION TUBES

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO. (BROKEN BOW)·Product code JKA·July 5, 2019