MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 06 report with the FDA on 2000-02-25 for DEROYAL COVADERM PLUS VAD DRESSING * 46-405 manufactured by Deroyal Industries, Inc..
[205508]
While removing the dressing, it causes the first layer of the skin to tear. This altered skin integrity.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1123071-2000-00005 |
MDR Report Key | 265305 |
Report Source | 06 |
Date Received | 2000-02-25 |
Date of Report | 2000-02-21 |
Report Date | 2000-02-21 |
Date Reported to FDA | 2000-02-21 |
Date Mfgr Received | 2000-01-26 |
Device Manufacturer Date | 1999-12-01 |
Date Added to Maude | 2000-02-29 |
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 Street | 200 DEBUSK LN |
Manufacturer City | POWELL TN 37849 |
Manufacturer Country | US |
Manufacturer Postal | 37849 |
Manufacturer Phone | 8659387828 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | DEROYAL COVADERM PLUS VAD DRESSING |
Generic Name | WOUND DRESSING |
Product Code | MSA |
Date Received | 2000-02-25 |
Returned To Mfg | 2000-02-01 |
Model Number | * |
Catalog Number | 46-405 |
Lot Number | 289980 |
ID Number | * |
Device Expiration Date | 2004-12-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | 1 MO |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 256843 |
Manufacturer | DEROYAL INDUSTRIES, INC. |
Manufacturer Address | 200 DEBUSK LANE POWELL TN 37849 US |
Baseline Brand Name | DEROYAL COVADERM PLUS VAD DRESSING |
Baseline Generic Name | WOUND DRESSING |
Baseline Model No | NA |
Baseline Catalog No | 46-405 |
Baseline ID | NA |
Baseline Device Family | WOUND DRESSING |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 60 |
Baseline PMA Flag | N |
Baseline 510K PMN | Y |
Premarket Notification | K910657 |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2000-02-25 |