MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,o report with the FDA on 2019-09-13 for BAKRI TAMPONADE BALLOON CATHETER G30673 J-SOS-100500 manufactured by Cook Inc.
Report Number | 1820334-2019-02309 |
MDR Report Key | 9033341 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,O |
Date Received | 2019-09-13 |
Date of Report | 2019-10-21 |
Date of Event | 2019-06-03 |
Date Mfgr Received | 2019-10-18 |
Device Manufacturer Date | 2017-07-24 |
Date Added to Maude | 2019-09-13 |
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. LARRY POOL |
Manufacturer Street | 750 DANIELS WAY |
Manufacturer City | BLOOMINGTON IN 47404 |
Manufacturer Country | US |
Manufacturer Postal | 47404 |
Manufacturer Phone | 8123392235 |
Manufacturer G1 | COOK INC |
Manufacturer Street | 750 DANIELS WAY |
Manufacturer City | BLOOMINGTON IN 47404 |
Manufacturer Country | US |
Manufacturer Postal Code | 47404 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | BAKRI TAMPONADE BALLOON CATHETER |
Generic Name | OQY INTRAUTERINE BALLOON |
Product Code | OQY |
Date Received | 2019-09-13 |
Returned To Mfg | 2019-10-03 |
Model Number | G30673 |
Catalog Number | J-SOS-100500 |
Lot Number | 8087300 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COOK INC |
Manufacturer Address | 750 DANIELS WAY BLOOMINGTON IN 47404 US 47404 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-09-13 |