15 results · 19ms · Sources: EU EUDAMED, US FDA

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SUCTION IRRIGATION CAUTERY PROBE

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

CELL-DYN

FDA UDI
ABBOTT LABORATORIES·00380740072445·CELL-DYN 1800 System DILUENT

APEX Knee System

FDA UDI
Omni Life Science, Inc.·00841690126461·Adjustable Modular Tibia Tray Trial Size 2

OTS - Class B 21 Field Trauma - Hawkespack

FDA UDI
Certified Safety Manufacturing, Inc.·00766588620022·OTS - Class B 21 Field Trauma - Hawkespack

Persyst 15 EEG Review and Analysis Software

FDA 510(k)
FDA Class 2 ·Neurology

SYDNEY IVF CULTURE OIL

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

INTERSTIM II

FDA Adverse Event
Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·November 16, 2012

INTERSTIM II

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code EZW·February 6, 2013

THERMAL SENSORY ANALYZER (TSA-II)

FDA Adverse Event
Injury ·MEDOC LTD., ADVANCED MEDICAL SURGERY MEDISCENSE USA·Product code LQW·December 26, 2019

UNK

FDA Adverse Event
Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·January 4, 2013

CAPSUREFIX NOVUS

FDA Adverse Event
Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 13, 2010

TELIGEN

FDA Adverse Event
Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·July 9, 2014

RESTORE PRIME

FDA Adverse Event
Injury ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LGW·April 25, 2024

QSENSE CPM THERMAL SENSORY ANALYZER 2001

FDA Adverse Event
Malfunction ·MEDOC LTD, ADVANCED MEDICAL SYSTEM·Product code LQW·April 19, 2022

CELL-DYN 1800 ANALYZER

FDA Adverse Event
Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKZ·January 26, 2009