MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-30 for PISCES Z QUAD 3890 manufactured by Given Imaging Los Angeles Llc.
Report Number | 3005344223-2020-00003 |
MDR Report Key | 9900281 |
Report Source | COMPANY REPRESENTATIVE,FOREIG |
Date Received | 2020-03-30 |
Date of Report | 2020-03-30 |
Date of Event | 2020-03-09 |
Date Mfgr Received | 2020-03-10 |
Device Manufacturer Date | 2018-03-20 |
Date Added to Maude | 2020-03-30 |
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 | AMY BEEMAN |
Manufacturer Street | 161 CHESHIRE LANE, SUITE 100 |
Manufacturer City | PLYMOUTH MN 55441 |
Manufacturer Country | US |
Manufacturer Postal | 55441 |
Manufacturer Phone | 7632104064 |
Manufacturer G1 | GIVEN IMAGING LOS ANGELES LLC |
Manufacturer Street | 5860 UPLANDER WAY |
Manufacturer City | CULVER CITY CA 90230 |
Manufacturer Country | US |
Manufacturer Postal Code | 90230 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | PISCES Z QUAD |
Generic Name | STIMULATOR, SPINAL-CORD, IMPLANTED (PAIN RELIEF) |
Product Code | GZB |
Date Received | 2020-03-30 |
Model Number | 3890 |
Catalog Number | 3890 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | GIVEN IMAGING LOS ANGELES LLC |
Manufacturer Address | 5860 UPLANDER WAY CULVER CITY CA 90230 US 90230 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-30 |