MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-05-22 for FG GATEWAY OTW JP 2.50MM X 9MM M0032072009250 manufactured by Boston Scientific - Minn.
        [109003786]
The subject device is not available.
 Patient Sequence No: 1, Text Type: N, H10
        [109003787]
It was reported that the subject balloon catheter was ruptured during procedure. There were no clinical consequences reported to the patient. No other information was provided.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3008853977-2018-00026 | 
| MDR Report Key | 7535308 | 
| Report Source | HEALTH PROFESSIONAL | 
| Date Received | 2018-05-22 | 
| Date of Report | 2018-07-25 | 
| Date of Event | 2018-04-27 | 
| Date Mfgr Received | 2018-06-27 | 
| Device Manufacturer Date | 2016-12-02 | 
| Date Added to Maude | 2018-05-22 | 
| 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 | MR. TARA LOPEZ | 
| Manufacturer Street | 47900 BAYSIDE PARKWAY | 
| Manufacturer City | FREMONT CA 94538 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 94538 | 
| Manufacturer Phone | 5104132500 | 
| Manufacturer G1 | BOSTON SCIENTIFIC - MINN | 
| Manufacturer Street | ONE SCIMED PLACE | 
| Manufacturer City | MAPLE GROVE MN 55311 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 55311 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | FG GATEWAY OTW JP 2.50MM X 9MM | 
| Generic Name | CATHETER, BALLOON TYPE | 
| Product Code | GBA | 
| Date Received | 2018-05-22 | 
| Catalog Number | M0032072009250 | 
| Lot Number | 20032574 | 
| Device Expiration Date | 2019-12-31 | 
| Operator | HEALTH PROFESSIONAL | 
| Device Availability | N | 
| Device Age | DA | 
| Device Eval'ed by Mfgr | R | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | BOSTON SCIENTIFIC - MINN | 
| Manufacturer Address | ONE SCIMED PLACE MAPLE GROVE MN 55311 US 55311 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 2018-05-22 |