MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-08-15 for GNG (GRAB ?N GO) OPTI E-CYLINDER manufactured by Praxair Distribution, Inc..
Report Number | 8896376 |
MDR Report Key | 8896376 |
Date Received | 2019-08-15 |
Date of Report | 2019-07-22 |
Date of Event | 2019-05-13 |
Report Date | 2019-08-06 |
Date Reported to FDA | 2019-08-06 |
Date Reported to Mfgr | 2019-08-15 |
Date Added to Maude | 2019-08-15 |
Event Key | 0 |
Report Source Code | User Facility report |
Manufacturer Link | N |
Number of Patients in Event | 0 |
Adverse Event Flag | 0 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | GNG (GRAB ?N GO) OPTI E-CYLINDER |
Generic Name | REGULATOR, PRESSURE, GAS CYLINDER |
Product Code | CAN |
Date Received | 2019-08-15 |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | PRAXAIR DISTRIBUTION, INC. |
Manufacturer Address | 175 E PARK DR TONAWANDA NY 14150 US 14150 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-15 |