MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-06-07 for PHOX ULTRA COOX 42013 manufactured by Nova Biomedical Corp..
| Report Number | 1219029-2019-00020 |
| MDR Report Key | 8680646 |
| Date Received | 2019-06-07 |
| Date of Report | 2019-06-07 |
| Date of Event | 2019-05-18 |
| Date Mfgr Received | 2019-05-19 |
| Date Added to Maude | 2019-06-07 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | MS. TAYLOR WARD |
| Manufacturer Street | 200 PROSPECT ST |
| Manufacturer City | WALTHAM MA 024543465 |
| Manufacturer Country | US |
| Manufacturer Postal | 024543465 |
| Manufacturer Phone | 7816473700 |
| Manufacturer G1 | NOVA BIOMEDICAL CORP. |
| Manufacturer Street | 200 PROSPECT ST |
| Manufacturer City | WALTHAM MA 024543465 |
| Manufacturer Country | US |
| Manufacturer Postal Code | 024543465 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 0 |
| Brand Name | PHOX ULTRA COOX |
| Generic Name | ELECTRODE MEASUREMENT, BLOOD-GASES (PCO2, PO2) AND BLOOD PH, |
| Product Code | CGZ |
| Date Received | 2019-06-07 |
| Model Number | 42013 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | NOVA BIOMEDICAL CORP. |
| Manufacturer Address | 200 PROSPECT ST WALTHAM MA 024543465 US 024543465 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-06-07 |