MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 01,02,05,07 report with the FDA on 2012-10-19 for IDRT-TS (INTL) SINGLE 4X5 84051 manufactured by Integra Lifesciences Corp..
[3095603]
The reporter noted the pt was enrolled in a clinical study in france titled: "eval of integra artificial dermis for the treatment of leg ulcers. Implantation of idrt was on (b)(6) 2011 on a venous ulcer from 2010. The pt developed a local infection and 'smelling flow under the silicone'. Antibiotic treatment was provided and the wound healed on (b)(6) 2011. "
Patient Sequence No: 1, Text Type: D, B5
[10430436]
The device involved in the reported incident is not available for eval. An investigation has been initiated based on the reported info.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 1121308-2012-00031 |
MDR Report Key | 2802354 |
Report Source | 01,02,05,07 |
Date Received | 2012-10-19 |
Date of Report | 2012-10-19 |
Date Mfgr Received | 2012-09-27 |
Date Added to Maude | 2012-10-25 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | CAREN FERNANDEZ |
Manufacturer Street | 315 ENTERPRISE DR |
Manufacturer City | PLAINSBORO NJ 08536 |
Manufacturer Country | US |
Manufacturer Postal | 08536 |
Manufacturer Phone | 6099362341 |
Single Use | 0 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | IDRT-TS (INTL) SINGLE 4X5 |
Generic Name | IDRT-TS |
Product Code | MGR |
Date Received | 2012-10-19 |
Catalog Number | 84051 |
Lot Number | 105C00203665 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INTEGRA LIFESCIENCES CORP. |
Manufacturer Address | PLAINSBORO NJ 08536 US 08536 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2012-10-19 |