MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2019-10-11 for PHOTOFIX PATCH - 6CM X 8CM PFP 6X8 PFP 6x8 manufactured by Cryolife, Inc..
Report Number | 1063481-2019-00060 |
MDR Report Key | 9180933 |
Report Source | DISTRIBUTOR,HEALTH PROFESSION |
Date Received | 2019-10-11 |
Date of Report | 2019-10-11 |
Date of Event | 2019-07-19 |
Date Facility Aware | 2019-08-16 |
Date Mfgr Received | 2019-08-16 |
Date Added to Maude | 2019-10-11 |
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 | 3 |
Event Location | 3 |
Manufacturer Contact | ROCHELLE MANEY |
Manufacturer Street | 1655 ROBERTS BLVD., NW |
Manufacturer City | KENNESAW GA 30144 |
Manufacturer Country | US |
Manufacturer Postal | 30144 |
Manufacturer Phone | 7704193355 |
Manufacturer G1 | CRYOLIFE, INC. |
Manufacturer Street | 1655 ROBERTS BLVD. NW |
Manufacturer City | KENNESAW GA 30144 |
Manufacturer Country | US |
Manufacturer Postal Code | 30144 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PHOTOFIX PATCH - 6CM X 8CM |
Generic Name | PHOTOFIX DECELLULARIZED BOVINE PERICARDIUM |
Product Code | PSQ |
Date Received | 2019-10-11 |
Model Number | PFP 6X8 |
Catalog Number | PFP 6x8 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CRYOLIFE, INC. |
Manufacturer Address | 1655 ROBERTS BLVD. NW KENNESAW GA 30144 US 30144 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2019-10-11 |