MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-07-18 for BRIGHTVIEW SPECT 2170-3000A 882480 manufactured by Philips Medical Systems (cleveland), Inc..
| Report Number | 1525965-2019-00045 |
| MDR Report Key | 8804239 |
| Date Received | 2019-07-18 |
| Date of Report | 2019-05-28 |
| Date Mfgr Received | 2019-05-28 |
| Date Added to Maude | 2019-07-18 |
| 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 | MR. DERRICK MASSURI |
| Manufacturer Street | 595 MINER RD |
| Manufacturer City | CLEVELAND OH 44143 |
| Manufacturer Country | US |
| Manufacturer Postal | 44143 |
| Manufacturer Phone | 4404833000 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Removal Correction Number | 1525965-06/11/2019-002-C |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | BRIGHTVIEW SPECT |
| Generic Name | SYSTEM, TOMOGRAPHY, COMPUTED, EMISSION |
| Product Code | KPS |
| Date Received | 2019-07-18 |
| Model Number | 2170-3000A |
| Catalog Number | 882480 |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | Y |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PHILIPS MEDICAL SYSTEMS (CLEVELAND), INC. |
| Manufacturer Address | 595 MINER RD CLEVELAND OH 44143 US 44143 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 2019-07-18 |