MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2019-10-14 for PHILIPS AVENT NIPPLE PROTECTOR SCF156 manufactured by Philips Electronics Uk Limited.
| Report Number | 8021997-2019-00004 |
| MDR Report Key | 9188793 |
| Date Received | 2019-10-14 |
| Date of Report | 2019-09-20 |
| Date Mfgr Received | 2019-11-01 |
| Date Added to Maude | 2019-10-14 |
| 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 | MS. NINA RUIZ |
| Manufacturer Street | 1600 SUMMER STREET |
| Manufacturer City | STAMFORD CT 06912 |
| Manufacturer Country | US |
| Manufacturer Postal | 06912 |
| Manufacturer G1 | PHILIPS ELECTRONICS UK LIMITED |
| Manufacturer Street | LOWER ROAD |
| Manufacturer City | GLEMSFORD, CO107QS |
| Manufacturer Country | UK |
| Manufacturer Postal Code | CO10 7QS |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Brand Name | PHILIPS AVENT NIPPLE PROTECTOR |
| Generic Name | NIPPLE PROTECTOR |
| Product Code | HFS |
| Date Received | 2019-10-14 |
| Returned To Mfg | 2019-10-25 |
| Model Number | SCF156 |
| Device Availability | R |
| Device Age | DA |
| Device Eval'ed by Mfgr | Y |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | PHILIPS ELECTRONICS UK LIMITED |
| Manufacturer Address | LOWER ROAD GLEMSFORD, CO107QS UK CO10 7QS |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Other | 2019-10-14 |