MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05 report with the FDA on 2002-03-22 for ADCON-L ANTI-ADHESION BARRIER GEL G0026 manufactured by Gliatech Medical Inc..
[21247148]
In 2/2002, a gliatech employee attended a professional meeting. During the meeting, dr. Reported on his experience with adcon-l. Dr. Mentioned that he had one pt with poor healing of the skin following application 2. 5 mg of adcon-l. No additional info is available at this time.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 1530649-2002-00006 |
MDR Report Key | 384140 |
Report Source | 05 |
Date Received | 2002-03-22 |
Date of Report | 2002-03-22 |
Date Mfgr Received | 2002-02-23 |
Date Added to Maude | 2002-03-26 |
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 | 0 |
Manufacturer Street | 23420 COMMERCE PARK ROAD |
Manufacturer City | CLEVELAND OH 44122 |
Manufacturer Country | US |
Manufacturer Postal | 44122 |
Manufacturer Phone | 2168313200 |
Manufacturer G1 | * |
Manufacturer Street | * |
Manufacturer City | * |
Manufacturer Country | * |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ADCON-L ANTI-ADHESION BARRIER GEL |
Generic Name | INHIBITOR, PERIDURAL |
Product Code | MLQ |
Date Received | 2002-03-22 |
Model Number | NA |
Catalog Number | G0026 |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | NA |
Device Eval'ed by Mfgr | R |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 373187 |
Manufacturer | GLIATECH MEDICAL INC. |
Manufacturer Address | 23420 COMMERCE PARK RD CLEVELAND OH 44122 US |
Baseline Brand Name | ADCON-L ADHESION CONTROL IN A BARRIER GEL |
Baseline Generic Name | INHIBITOR, PERIDURAL FIBROSIS |
Baseline Model No | NA |
Baseline Catalog No | G0026 |
Baseline ID | 3 GRAMS IN SYRI |
Baseline Device Family | ADCON-L ADHESION CONTROL IN A BARRIER GEL |
Baseline Shelf Life Contained | Y |
Baseline Shelf Life [Months] | 24 |
Baseline PMA Flag | Y |
Premarket Approval | P9600 |
Baseline 510K PMN | N |
Baseline Preamendment | N |
Baseline Transitional | N |
510k Exempt | N |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2002-03-22 |