MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,foreign,other report with the FDA on 2020-03-20 for FRESHLOOK ONE-DAY CBV92013371 manufactured by Ciba Vision Gmbh.
Report Number | 9610813-2020-00005 |
MDR Report Key | 9862341 |
Report Source | DISTRIBUTOR,FOREIGN,OTHER |
Date Received | 2020-03-20 |
Date of Report | 2020-03-31 |
Date of Event | 2020-01-27 |
Date Mfgr Received | 2020-03-30 |
Device Manufacturer Date | 2019-07-21 |
Date Added to Maude | 2020-03-20 |
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 | MR. JONATHAN SCHLECH |
Manufacturer Street | 6201 SOUTH FREEWAY MAIL STOP AB2-6 |
Manufacturer City | FORT WORTH TX 76134 |
Manufacturer Country | US |
Manufacturer Postal | 76134 |
Manufacturer Phone | 8175514979 |
Manufacturer G1 | CIBA VISION GMBH |
Manufacturer Street | POSTFACH, INDUSTRIERING 1 |
Manufacturer City | GROSSWALLSTADT D-63868 |
Manufacturer Country | GM |
Manufacturer Postal Code | D-63868 |
Single Use | 3 |
Previous Use Code | 3 |
Removal Correction Number | NA |
Event Type | 3 |
Type of Report | 3 |
Brand Name | FRESHLOOK ONE-DAY |
Generic Name | LENS, CONTACT, (DISPOSABLE) |
Product Code | MVN |
Date Received | 2020-03-20 |
Model Number | NA |
Catalog Number | CBV92013371 |
Lot Number | N0684902 |
Operator | LAY USER/PATIENT |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CIBA VISION GMBH |
Manufacturer Address | POSTFACH, INDUSTRIERING 1 GROSSWALLSTADT D-63868 GM D-63868 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-20 |