MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2019-06-17 for SPF PLUS-MINI (60 ?A/M) N/A 10-1398M manufactured by Ebi, Llc..
Report Number | 0002242816-2019-00018 |
MDR Report Key | 8705747 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-06-17 |
Date of Report | 2019-07-05 |
Date of Event | 2019-05-30 |
Date Mfgr Received | 2019-07-03 |
Device Manufacturer Date | 2019-01-24 |
Date Added to Maude | 2019-06-17 |
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 | SHAAN POLIUS |
Manufacturer Street | 399 JEFFERSON ROAD |
Manufacturer City | PARSIPPANY NJ 07054 |
Manufacturer Country | US |
Manufacturer Postal | 07054 |
Manufacturer Phone | 9732999300 |
Manufacturer G1 | EBI, LLC. |
Manufacturer Street | 399 JEFFERSON ROAD |
Manufacturer City | PARSIPPANY NJ 07054 |
Manufacturer Country | US |
Manufacturer Postal Code | 07054 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | N/A |
Event Type | 3 |
Type of Report | 3 |
Brand Name | SPF PLUS-MINI (60 ?A/M) |
Generic Name | SPF-PLUS 60/M, SPINAL FUSION STIMULATOR |
Product Code | LOE |
Date Received | 2019-06-17 |
Model Number | N/A |
Catalog Number | 10-1398M |
Lot Number | N/A |
Operator | LAY USER/PATIENT |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | EBI, LLC. |
Manufacturer Address | 399 JEFFERSON ROAD PARSIPPANY NJ 07054 US 07054 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2019-06-17 |