MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,user faci report with the FDA on 2017-03-28 for VISCO360 VISCOSURGICAL SYSTEM 03916 manufactured by Sight Sciences, Inc..
[71215584]
All pertinent information available to sight sciences, inc. Has been submitted. The company is submitting this mdr to ensure full compliance with 21 cfr 803. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[71215585]
The surgeon reported that the tip of the microcatheter was severed while performing visco-dilation. The microcatheter separated from the device when retracting it from schlemm's canal. The entire device was removed successfully from the eye. A new device was successfully used to complete the case. The event did not result in any adverse impact to the patient.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3010363671-2017-00012 |
MDR Report Key | 6439938 |
Report Source | HEALTH PROFESSIONAL,USER FACI |
Date Received | 2017-03-28 |
Date of Report | 2017-02-24 |
Date of Event | 2017-02-23 |
Date Mfgr Received | 2017-03-02 |
Device Manufacturer Date | 2016-12-27 |
Date Added to Maude | 2017-03-28 |
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 | ANNE-MARIE RIPLEY |
Manufacturer Street | 3000 SAND HILL ROAD, 3-105 |
Manufacturer City | MENLO PARK CA 94025 |
Manufacturer Country | US |
Manufacturer Postal | 94025 |
Manufacturer Phone | 6616458546 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | VISCO360 VISCOSURGICAL SYSTEM |
Generic Name | VISCOELASTIC INJECTOR |
Product Code | MRH |
Date Received | 2017-03-28 |
Returned To Mfg | 2017-02-27 |
Model Number | 03916 |
Catalog Number | 03916 |
Lot Number | 1005191 |
Device Expiration Date | 2017-12-31 |
Operator | PHYSICIAN |
Device Availability | R |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | SIGHT SCIENCES, INC. |
Manufacturer Address | 3000 SAND HILL ROAD, 3-105 MENLO PARK CA 94025 US 94025 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2017-03-28 |