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.
[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
Report Number | 1217116-2001-00017 |
MDR Report Key | 358040 |
Report Source | 06 |
Date Received | 2001-10-19 |
Date of Report | 2001-10-19 |
Date of Event | 2001-09-20 |
Report Date | 2001-10-19 |
Date Mfgr Received | 2001-09-25 |
Date Added to Maude | 2001-10-29 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | SARAH BAXTER |
Manufacturer Street | P.O. BOX 3828 |
Manufacturer City | * |
Manufacturer Country | * |
Manufacturer Phone | 4877665 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | TELESCOPING CEILING SUSPENSION |
Generic Name | DIAGNOSTIC X-RAY TUBE MOUNT |
Product Code | IYB |
Date Received | 2001-10-19 |
Model Number | 9848-500-23102 |
Catalog Number | NA |
Lot Number | NA |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | NO INFO |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 347253 |
Manufacturer | PHILIPS MEDEZIN SYSTEME |
Manufacturer Address | ROENTGENSTRASSE 24 HAMBURG GM 2000 |
Baseline Brand Name | TELESCOPE CARRIAGE CS |
Baseline Generic Name | DIAGNOSTIC X-RAY TUBE MOUNT |
Baseline Model No | 9848-500-23102 |
Baseline Catalog No | NA |
Baseline ID | NA |
Baseline Device Family | CS 62/64 |
Baseline Shelf Life [Months] | NA |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2001-10-19 |