MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-26 for ANALYZER SURGICAL CABLE 2292 manufactured by Cov Lp/llc, Augusta.
Report Number | 1018120-2020-00002 |
MDR Report Key | 9884098 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-26 |
Date of Report | 2020-03-26 |
Date of Event | 2020-02-10 |
Date Mfgr Received | 2020-03-25 |
Device Manufacturer Date | 2017-02-21 |
Date Added to Maude | 2020-03-26 |
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 | PAULA BIXBY |
Manufacturer Street | 8200 CORAL SEA ST NE |
Manufacturer City | MOUNDS VIEW MN 55112 |
Manufacturer Country | US |
Manufacturer Postal | 55112 |
Manufacturer Phone | 7635055378 |
Manufacturer G1 | COV LP/LLC, AUGUSTA |
Manufacturer Street | 1647 PERKINS RD |
Manufacturer City | AUGUSTA GA 30913 |
Manufacturer Country | US |
Manufacturer Postal Code | 30913 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ANALYZER SURGICAL CABLE |
Generic Name | PROGRAMMER, PACEMAKER |
Product Code | KRG |
Date Received | 2020-03-26 |
Returned To Mfg | 2020-02-27 |
Model Number | 2292 |
Catalog Number | 2292 |
Lot Number | 2292 |
Operator | HEALTH PROFESSIONAL |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | COV LP/LLC, AUGUSTA |
Manufacturer Address | 1647 PERKINS RD AUGUSTA GA 30913 US 30913 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-26 |