IMRIS ORT100 OPERATING ROOM TABLE ORT100 (T2) 108000-000

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2018-02-07 for IMRIS ORT100 OPERATING ROOM TABLE ORT100 (T2) 108000-000 manufactured by Imris - Deerfield Imaging, Inc..

Event Text Entries

[99824801] The table's rotational locking mechanism wa repaired by the service engineer. Internal capa issued.
Patient Sequence No: 1, Text Type: N, H10


[99824802] Service call scheduled for rotational lock repair. No patient involvement.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number3010326005-2018-00012
MDR Report Key7249585
Date Received2018-02-07
Date of Report2018-02-07
Date of Event2017-12-22
Date Mfgr Received2017-12-22
Device Manufacturer Date2007-10-11
Date Added to Maude2018-02-07
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 ContactMR TODD SPERLING
Manufacturer Street5101 SHADY OAK ROAD
Manufacturer CityMINNETONKA MN 553434100
Manufacturer CountryUS
Manufacturer Postal553434100
Manufacturer Phone7632036344
Manufacturer G1IMRIS - DEERFIELD IMAGING, INC.
Manufacturer Street5101 SHADY OAK ROAD
Manufacturer CityMINNETONKA MN 553434100
Manufacturer CountryUS
Manufacturer Postal Code553434100
Single Use3
Previous Use Code3
Event Type3
Type of Report0

Device Details

Brand NameIMRIS ORT100 OPERATING ROOM TABLE
Generic NameOPERATING ROOM TABLE
Product CodeKXJ
Date Received2018-02-07
Model NumberORT100 (T2)
Catalog Number108000-000
Lot NumberN/A
OperatorNURSE
Device AvailabilityY
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerIMRIS - DEERFIELD IMAGING, INC.
Manufacturer Address5101 SHADY OAK ROAD MINNETONKA MN 553434100 US 553434100


Patients

Patient NumberTreatmentOutcomeDate
10 2018-02-07

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