MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2004-03-05 for DIAGNOST 76 9848-500-16202 NA manufactured by Philips Medical Systems.
[309835]
Pt was undergoing a procedure on this x-ray system. Pt was lying face down with arms above head and fingers over table edge. The x-ray table top moved toward the foot of the table. The pt's left hand became caught between the underside of the table top and the cover of the longitudinal motor drive compartment. Pt's left hand fingers were pinched with a middle finger laceration.
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1217116-2004-00007 |
| MDR Report Key | 515122 |
| Report Source | 05 |
| Date Received | 2004-03-05 |
| Date of Report | 2004-02-09 |
| Date of Event | 2004-02-09 |
| Report Date | 2004-02-09 |
| Date Reported to FDA | 2004-03-05 |
| Date Mfgr Received | 2004-02-09 |
| Device Manufacturer Date | 1995-01-01 |
| Date Added to Maude | 2004-03-11 |
| 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 | 3 |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | DREW QUEEN |
| Manufacturer Street | 22100 BOTHELL EVERETT HWY |
| Manufacturer City | BOTHELL WA 98041 |
| Manufacturer Country | US |
| Manufacturer Postal | 98041 |
| Manufacturer Phone | 4254877199 |
| Manufacturer G1 | PHILIPS MEDICAL SYSTEMS |
| Manufacturer Street | ROENTGENSTRASSE 24 |
| Manufacturer City | HAMBURG 2000 |
| Manufacturer Country | GM |
| Manufacturer Postal Code | 2000 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | DIAGNOST 76 |
| Generic Name | RADIOGRAPHIC / FLUOROSCOPIC TABLE |
| Product Code | IXL |
| Date Received | 2004-03-05 |
| Model Number | 9848-500-16202 |
| Catalog Number | NA |
| Lot Number | NA |
| ID Number | * |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | 9 YR |
| Device Eval'ed by Mfgr | Y |
| Implant Flag | N |
| Date Removed | A |
| Device Sequence No | 1 |
| Device Event Key | 504132 |
| Manufacturer | PHILIPS MEDICAL SYSTEMS |
| Manufacturer Address | ROENTGENSTRASSE 24 HAMBURG GM 2000 |
| Baseline Brand Name | DIAGNOST 76 PLUS |
| Baseline Generic Name | GENERAL PURPOSE R/F SYSTEM (SPOT FILM/IMAGE INTENSIFIED) |
| Baseline Model No | 9848-500-16202 |
| Baseline Catalog No | NA |
| Baseline ID | NA |
| Baseline Device Family | DIAGNOST 76 FAMILY |
| Baseline Shelf Life [Months] | NA |
| Baseline PMA Flag | N |
| Baseline 510K PMN | Y |
| Premarket Notification | K924593 |
| Baseline Preamendment | N |
| Baseline Transitional | N |
| 510k Exempt | N |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other; 2. Required No Informationntervention | 2004-03-05 |