48 results · 23ms · Sources: EU EUDAMED, US FDA

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Manual Wheelchair, Model A011

FDA 510(k)
FDA Class 1 ·Physical Medicine

Puget Sound Energy - 18 Metal

FDA UDI
Certified Safety Manufacturing, Inc.·00766588014692·Puget Sound Energy - 18 Metal

Merit Medical®

FDA UDI
Merit Medical Systems, Inc.·00884450157626·

ATLANTIS VISION ANTERIOR CERVICAL PLATE SYSTEM

FDA 510(k)
FDA Class 2 ·Orthopedic

TPN NUTRITION BAG (EVA), EMPTYING TUBE, BAG SYRINGE FILL SET

FDA 510(k)
FDA Class 2 ·General Hospital

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·July 31, 2025

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·January 10, 2019

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code FOZ·February 24, 2022

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·February 4, 2022

BD VACUTAINER® PUSH BUTTON BLOOD COLLECTION SET WITH PRE-ATTACHED HOLDER

FDA Adverse Event
Malfunction ·BECTON, DICKINSON & CO., (BD)·Product code JKA·February 4, 2022

UNKNOWN DEPUY PRESERVATION ALLPOLY TIBIA

FDA Adverse Event
Injury ·DEPUY ORTHOPAEDICS, INC.·Product code HSH·October 16, 2008

CVC SET: 2-LUMEN 7FR X 2 0CM

FDA Adverse Event
Malfunction ·ARROW INTL., INC.·Product code FOZ·August 3, 2011

ACUVUE 2 BRAND CONTACT LENSES

FDA Adverse Event
Injury ·VISTAKON·Product code LPL·June 28, 2013

INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·July 2, 2018

BALL HEADS: MECTACER BIOLOX DELTA CERAMIC BALL HEAD 12/14 Ø 40 SIZE S

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 2, 2024

STEM: M-VIZION DISTAL STEM Ø14MM L 180MM STRAIGHT

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·August 9, 2023

ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWQ·June 13, 2018

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·March 3, 2025

M-VIZION FEMORAL REVISION SYSTEM

FDA Adverse Event
Injury ·MEDACTA INTERNATIONAL SA·Product code LZO·October 2, 2025