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 2020-03-04 for MAXI LD PTA F7 110 25X40 4162540L manufactured by Cordis Corporation.
Report Number | 9616099-2020-03550 |
MDR Report Key | 9786655 |
Report Source | COMPANY REPRESENTATIVE,HEALTH |
Date Received | 2020-03-04 |
Date of Report | 2020-03-09 |
Date of Event | 2020-02-05 |
Date Mfgr Received | 2020-03-09 |
Device Manufacturer Date | 2018-08-04 |
Date Added to Maude | 2020-03-04 |
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 | MRS. KARLA CASTRO |
Manufacturer Street | 14201 NW 60TH AVE |
Manufacturer City | MIAMI LAKES FL 33014 |
Manufacturer Country | US |
Manufacturer Postal | 33014 |
Manufacturer Phone | 7863138372 |
Manufacturer G1 | CORDIS CORPORATION |
Manufacturer Street | 14201 NW 60TH AVE |
Manufacturer City | MIAMI LAKES FL 33014 |
Manufacturer Country | US |
Manufacturer Postal Code | 33014 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MAXI LD PTA F7 110 25X40 |
Generic Name | DILATOR, ESOPHAGEAL |
Product Code | KNQ |
Date Received | 2020-03-04 |
Model Number | 4162540L |
Catalog Number | 4162540L |
Lot Number | 82156670 |
Device Expiration Date | 2020-01-31 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CORDIS CORPORATION |
Manufacturer Address | 14201 NW 60 AVENUE MIAMI LAKES FL 33014 US 33014 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2020-03-04 |