AMSCO 3080RC/RL SURGICAL TABLE 2175655

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2005-10-07 for AMSCO 3080RC/RL SURGICAL TABLE 2175655 manufactured by Steris Corporation.

MAUDE Entry Details

Report Number1043572-2005-00008
MDR Report Key643428
Report Source06
Date Received2005-10-07
Date of Report2005-10-06
Date of Event2005-09-07
Date Mfgr Received2005-09-28
Device Manufacturer Date1988-01-01
Date Added to Maude2005-11-01
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 Location0
Manufacturer ContactROBERT MCCALL
Manufacturer Street2720 GUNTER PARK DR EAST
Manufacturer CityMONTGOMERY AL 36109
Manufacturer CountryUS
Manufacturer Postal36109
Manufacturer Phone3342133150
Manufacturer G1STERIS CORPORATION - MONTGOMERY
Manufacturer Street2720 GUNTER PARK DR EAST
Manufacturer CityMONTGOMERY AL 36109
Manufacturer CountryUS
Manufacturer Postal Code36109
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAMSCO 3080RC/RL SURGICAL TABLE
Generic NameSURGICAL TABLES AND ACCESSORIES
Product CodeFSE
Date Received2005-10-07
Model Number3080RC
Catalog Number2175655
Lot NumberNA
ID NumberBE58-731
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Age17 YR
Device Eval'ed by MfgrR
Implant FlagN
Date Removed*
Device Sequence No1
Device Event Key632936
ManufacturerSTERIS CORPORATION
Manufacturer Address2720 GUNTER PARK EAST MONTGOMERY AL 36109 US
Baseline Brand NameAMSCO 3080RC/RL SURGICAL TABLE
Baseline Generic NameSURGICAL TABLES AND ACCESSORIES
Baseline Model No3080RC
Baseline Catalog No21`75655
Baseline IDBE58-731


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2005-10-07

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