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 2019-08-11 for RULER 71674079 manufactured by Smith & Nephew, Inc..
Report Number | 1020279-2019-02982 |
MDR Report Key | 8881878 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2019-08-11 |
Date of Report | 2019-09-18 |
Date of Event | 2019-07-13 |
Date Mfgr Received | 2019-07-13 |
Device Manufacturer Date | 2018-02-21 |
Date Added to Maude | 2019-08-11 |
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 | DR. SARAH FREESTONE |
Manufacturer Street | 1450 BROOKS ROAD |
Manufacturer City | MEMPHIS TN 38116 |
Manufacturer Country | US |
Manufacturer Postal | 38116 |
Manufacturer Phone | 0447940038 |
Manufacturer G1 | SMITH & NEPHEW, INC. |
Manufacturer Street | 1450 BROOKS ROAD |
Manufacturer City | MEMPHIS TN 38116 |
Manufacturer Country | US |
Manufacturer Postal Code | 38116 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | RULER |
Generic Name | TAPE, MEASURING, RULERS AND CALIPERS |
Product Code | FTY |
Date Received | 2019-08-11 |
Returned To Mfg | 2019-07-24 |
Catalog Number | 71674079 |
Lot Number | 18AYX0002 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SMITH & NEPHEW, INC. |
Manufacturer Address | 1450 BROOKS ROAD MEMPHIS TN 38116 US 38116 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-08-11 |