MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,consum report with the FDA on 2020-03-19 for XENFORM M0068302450 830-245 manufactured by Boston Scientific Corporation.
Report Number | 3005099803-2020-01056 |
MDR Report Key | 9857316 |
Report Source | COMPANY REPRESENTATIVE,CONSUM |
Date Received | 2020-03-19 |
Date of Report | 2020-03-19 |
Date of Event | 2011-06-24 |
Date Mfgr Received | 2020-02-19 |
Device Manufacturer Date | 2010-12-16 |
Date Added to Maude | 2020-03-19 |
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 | CAROLE MORLEY |
Manufacturer Street | 300 BOSTON SCIENTIFIC WAY |
Manufacturer City | MARLBOROUGH MA 01752 |
Manufacturer Country | US |
Manufacturer Postal | 01752 |
Manufacturer Phone | 5086834015 |
Manufacturer G1 | TEI BIOSCIENCES INCORPORATED |
Manufacturer Street | 7 ELKINS STREET |
Manufacturer City | BOSTON MA 02127 |
Manufacturer Country | US |
Manufacturer Postal Code | 02127 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | XENFORM |
Generic Name | MESH, SURGICAL, NON-SYNTHETIC, UROGYNECOLOGIC FOR APICAL VAGINAL AND UTERINE PRO |
Product Code | FTM |
Date Received | 2020-03-19 |
Model Number | M0068302450 |
Catalog Number | 830-245 |
Lot Number | 0001012011 |
Device Expiration Date | 2013-05-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | BOSTON SCIENTIFIC CORPORATION |
Manufacturer Address | 300 BOSTON SCIENTIFIC WAY MARLBOROUGH MA 01752 US 01752 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2020-03-19 |