MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a other report with the FDA on 2019-11-25 for INVACARE PLATINUM 10 OXYGEN CONCENTRATOR IRC10LXO2 manufactured by Invacare Florida.
Report Number | 1031452-2019-00107 |
MDR Report Key | 9370522 |
Report Source | OTHER |
Date Received | 2019-11-25 |
Date of Report | 2019-11-01 |
Date of Event | 2019-10-22 |
Date Mfgr Received | 2019-11-01 |
Device Manufacturer Date | 2010-10-01 |
Date Added to Maude | 2019-11-25 |
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. JASON FIEST |
Manufacturer Street | ONE INVACARE WAY |
Manufacturer City | ELYRIA OH 44035 |
Manufacturer Country | US |
Manufacturer Postal | 44035 |
Manufacturer Phone | 8003336900 |
Manufacturer G1 | INVACARE FLORIDA |
Manufacturer Street | 2101 EAST LAKE MARY BLVD |
Manufacturer City | SANFORD FL 32773 |
Manufacturer Country | US |
Manufacturer Postal Code | 32773 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | INVACARE PLATINUM 10 OXYGEN CONCENTRATOR |
Generic Name | GENERATOR, OXYGEN, PORTABLE |
Product Code | CAW |
Date Received | 2019-11-25 |
Model Number | IRC10LXO2 |
Catalog Number | IRC10LXO2 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | INVACARE FLORIDA |
Manufacturer Address | 2101 EAST LAKE MARY BLVD SANFORD FL 32773 US 32773 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-25 |