TELESCOPING CEILING SUSPENSION 9848-500-23102 NA

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 2001-10-19 for TELESCOPING CEILING SUSPENSION 9848-500-23102 NA manufactured by Philips Medezin Systeme.

Event Text Entries

[233561] The cover of the ceiling crane (cs2) fell off, striking the x-ray tech in the face. The tech reported a bruise on the left shoulder, wrist and hand, the left eye was bruised and there was a small laceration under the left eye. No bones were fractured due to contact with the cover.
Patient Sequence No: 1, Text Type: D, B5


MAUDE Entry Details

Report Number1217116-2001-00017
MDR Report Key358040
Report Source06
Date Received2001-10-19
Date of Report2001-10-19
Date of Event2001-09-20
Report Date2001-10-19
Date Mfgr Received2001-09-25
Date Added to Maude2001-10-29
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag0
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactSARAH BAXTER
Manufacturer StreetP.O. BOX 3828
Manufacturer City*
Manufacturer Country*
Manufacturer Phone4877665
Manufacturer G1*
Manufacturer Street*
Manufacturer City*
Manufacturer Country*
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTELESCOPING CEILING SUSPENSION
Generic NameDIAGNOSTIC X-RAY TUBE MOUNT
Product CodeIYB
Date Received2001-10-19
Model Number9848-500-23102
Catalog NumberNA
Lot NumberNA
ID Number*
OperatorHEALTH PROFESSIONAL
Device AvailabilityY
Device AgeNO INFO
Device Eval'ed by MfgrY
Implant FlagN
Date RemovedA
Device Sequence No1
Device Event Key347253
ManufacturerPHILIPS MEDEZIN SYSTEME
Manufacturer AddressROENTGENSTRASSE 24 HAMBURG GM 2000
Baseline Brand NameTELESCOPE CARRIAGE CS
Baseline Generic NameDIAGNOSTIC X-RAY TUBE MOUNT
Baseline Model No9848-500-23102
Baseline Catalog NoNA
Baseline IDNA
Baseline Device FamilyCS 62/64
Baseline Shelf Life [Months]NA
Baseline PMA FlagN
Baseline 510K PMNN
Baseline PreamendmentN
Baseline TransitionalN
510k ExemptY


Patients

Patient NumberTreatmentOutcomeDate
101. Other 2001-10-19

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