MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,06 report with the FDA on 1998-04-29 for BLADE RING LEFT SIZE 5 N7519 L5 manufactured by Storz Instrument Company.
[17414475]
This blade broke while being used on a pt. Another ring was used. There was no pt injury.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1932180-1998-00025 |
MDR Report Key | 165376 |
Report Source | 05,06 |
Date Received | 1998-04-29 |
Date of Report | 1998-04-02 |
Date of Event | 1998-03-30 |
Date Facility Aware | 1998-03-30 |
Report Date | 1998-04-02 |
Date Reported to Mfgr | 1998-04-02 |
Date Mfgr Received | 1998-04-02 |
Date Added to Maude | 1998-05-04 |
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 | BLADE RING LEFT SIZE 5 |
Generic Name | MOUTH GAG |
Product Code | KBN |
Date Received | 1998-04-29 |
Model Number | NA |
Catalog Number | N7519 L5 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | UNKNOWN |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 160957 |
Manufacturer | STORZ INSTRUMENT COMPANY |
Manufacturer Address | 499 SOVEREIGN CT. ST LOUIS MO 63011 US |
Baseline Brand Name | BLADE RING LEFT SIZE 5 |
Baseline Generic Name | MOUTH GAG |
Baseline Model No | NA |
Baseline Catalog No | N7519 L5 |
Baseline ID | NA |
Baseline Device Family | MOUTH GAG |
Baseline Shelf Life Contained | A |
Baseline PMA Flag | N |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | Y |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1998-04-29 |