T-MAX ESCHMANN/JAP TABLES TENET 7407 72200481

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-10-24 for T-MAX ESCHMANN/JAP TABLES TENET 7407 72200481 manufactured by Smith & Nephew, Inc..

MAUDE Entry Details

Report Number1643264-2019-00725
MDR Report Key9233308
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-10-24
Date of Report2019-11-20
Date of Event2019-09-26
Date Mfgr Received2019-11-19
Date Added to Maude2019-10-24
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 ContactHOLLY TOPPING
Manufacturer Street7000 WEST WILLIAM CANNON DRIVE
Manufacturer CityAUSTIN TX 78735
Manufacturer CountryUS
Manufacturer Postal78735
Manufacturer Phone5123913905
Manufacturer G1SMITH & NEPHEW, INC.
Manufacturer Street76 S. MERIDIAN AVE.
Manufacturer CityOKLAHOMA CITY OK 731076512
Manufacturer CountryUS
Manufacturer Postal Code731076512
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameT-MAX ESCHMANN/JAP TABLES TENET 7407
Generic NameACCESSORIES, OPERATING-ROOM, TABLE (KIT)
Product CodeFWZ
Date Received2019-10-24
Catalog Number72200481
Lot NumberUNKNOWN
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device AgeDA
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerSMITH & NEPHEW, INC.
Manufacturer Address76 S. MERIDIAN AVE. OKLAHOMA CITY OK 731076512 US 731076512


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2019-10-24

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