35 results · 27ms · Sources: EU EUDAMED, US FDA

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DIASORIN LIAISON TREPONEMA ASSAY

FDA 510(k)
FDA Class 2 ·Microbiology

BioQuick®

FDA UDI
Forestadent Bernhard Förster GmbH·EFOR70612471·BioQuick-Brackets FACE Evolution II System .022...

HOLY DRAGON STERILE ACUPUNCTURE NEEDLE FOR SINGLE USE

FDA 510(k)
FDA Class 2 ·General Hospital

PNEUMOPERITONEUM INSUFFLATION NEEDLE

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

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code KWQ·December 2, 2011

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDICS·Product code KWQ·April 16, 2018

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·October 30, 2009

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·October 7, 2015

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·September 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·September 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·October 9, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·October 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·September 11, 2019

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK·Product code HWC·October 29, 2009

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·WARSAW ORTHOPEDICS·Product code KWQ·January 3, 2013

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Malfunction ·MEDTRONIC SOFAMOR DANEK PUERTO RICO OPERATIONS·Product code KWQ·August 12, 2011

EVERCROSS¿ .035" OTW PTA DILATATION CATHETER

FDA Adverse Event
Injury ·EV3 INC.·Product code DQY·April 16, 2013

FREESTYLE

FDA Adverse Event
Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·June 19, 2008

NI

FDA Adverse Event
Injury ·SYNTHES (USA)·Product code HSB·April 11, 2011

VENTURE ANTERIOR CERVICAL PLATE SYSTEM

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWQ·December 11, 2009