MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06,07 report with the FDA on 1996-11-22 for AUTO BOX DL 6200 767215 manufactured by Sensormedics Corp..
[17481453]
In the model 6200, a capacitor on the co2 analyzer assembly burned up. There were no injuries and no pt involvement.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2050001-1996-00032 |
MDR Report Key | 53658 |
Report Source | 05,06,07 |
Date Received | 1996-11-22 |
Date of Report | 1996-11-20 |
Date of Event | 1996-11-01 |
Date Mfgr Received | 1996-11-01 |
Device Manufacturer Date | 1996-02-01 |
Date Added to Maude | 1996-12-06 |
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 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AUTO BOX DL |
Generic Name | BODY PLETHYSMOGRAPH |
Product Code | JEH |
Date Received | 1996-11-22 |
Returned To Mfg | 1996-11-08 |
Model Number | 6200 |
Catalog Number | 767215 |
Lot Number | NA |
ID Number | * |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | * |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 54257 |
Manufacturer | SENSORMEDICS CORP. |
Manufacturer Address | 22705 SAVI RANCH PARKWAY YORBA LINDA CA 928874645 US |
Baseline Brand Name | AUTOBOX DL |
Baseline Generic Name | BODY PLETHYSMOGRAPH |
Baseline Model No | 6200 |
Baseline Catalog No | 767215 |
Baseline ID | NA |
Baseline Device Family | NA |
Baseline Shelf Life Contained | A |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K923989 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1996-11-22 |