DUO HEADLIGHT 2 BAY SYSTEM - US 90620US

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,user f report with the FDA on 2019-08-25 for DUO HEADLIGHT 2 BAY SYSTEM - US 90620US manufactured by Integra Lifesciences Corp.

MAUDE Entry Details

Report Number2523190-2019-00102
MDR Report Key8928806
Report SourceCOMPANY REPRESENTATIVE,USER F
Date Received2019-08-25
Date of Report2019-07-29
Date of Event2019-07-20
Date Mfgr Received2019-09-17
Date Added to Maude2019-08-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMRS. KIMBERLY SHELLY
Manufacturer Street311 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal08536
Manufacturer Phone6099362319
Manufacturer G1INTEGRA LIFESCIENCES CORP
Manufacturer Street311 ENTERPRISE DRIVE
Manufacturer CityPLAINSBORO NJ 08536
Manufacturer CountryUS
Manufacturer Postal Code08536
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameDUO HEADLIGHT 2 BAY SYSTEM - US
Generic NamePFM05
Product CodeFSR
Date Received2019-08-25
Catalog Number90620US
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerINTEGRA LIFESCIENCES CORP
Manufacturer Address311 ENTERPRISE DRIVE 311 ENTERPRISE DRIVE PLAINSBORO NJ 08536 US 08536


Patients

Patient NumberTreatmentOutcomeDate
10 2019-08-25

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