MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 1996-11-12 for 7.5V TRANSFORMER N1011 manufactured by Storz Instrument Company.
[30390]
This transformer does not have a ground wire. This problem was found upon incoming inspection.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1932180-1996-00105 |
MDR Report Key | 48692 |
Report Source | 06 |
Date Received | 1996-11-12 |
Date of Report | 1996-10-14 |
Date of Event | 1996-10-14 |
Date Facility Aware | 1996-10-14 |
Report Date | 1996-10-14 |
Date Reported to Mfgr | 1996-10-14 |
Date Mfgr Received | 1996-10-14 |
Date Added to Maude | 1996-11-15 |
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 | 7.5V TRANSFORMER |
Generic Name | TRANSFORMER |
Product Code | HPQ |
Date Received | 1996-11-12 |
Model Number | NA |
Catalog Number | N1011 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | * |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 49456 |
Manufacturer | STORZ INSTRUMENT COMPANY |
Manufacturer Address | 499 SOVEREIGN COURT ST LOUIS MO 63601 US |
Baseline Brand Name | STORZ 7.5V TRANSFORMER |
Baseline Generic Name | TRANSFORMER |
Baseline Model No | NA |
Baseline Catalog No | N1011 |
Baseline ID | NA |
Baseline Device Family | HEADLIGHT TRANSFORMER |
Baseline Shelf Life Contained | N |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1996-11-12 |