MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a distributor,health profession report with the FDA on 2019-11-27 for HEALON ENDOCOAT VT585U manufactured by Johnson & Johnson Surgical Vision, Inc..
Report Number | 3004750704-2019-00087 |
MDR Report Key | 9385980 |
Report Source | DISTRIBUTOR,HEALTH PROFESSION |
Date Received | 2019-11-27 |
Date of Report | 2019-11-27 |
Report Date | 2005-01-01 |
Date Reported to FDA | 2005-01-01 |
Date Reported to Mfgr | 2005-01-10 |
Date Mfgr Received | 2019-10-30 |
Device Manufacturer Date | 2019-03-06 |
Date Added to Maude | 2019-11-27 |
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 | SOMYATA NAGPAL |
Manufacturer Street | 1700 EAST ST. ANDREW PLACE |
Manufacturer City | SANTA ANA CA 92705 |
Manufacturer Country | US |
Manufacturer Postal | 92705 |
Manufacturer Phone | 7142478200 |
Manufacturer G1 | JOHNSON & JOHNSON SURGICAL VISION, INC. |
Manufacturer Street | RAPSGATAN |
Manufacturer City | UPPSALA 751 82 |
Manufacturer Country | SE |
Manufacturer Postal Code | 751 82 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | HEALON ENDOCOAT |
Generic Name | OVDS |
Product Code | LZP |
Date Received | 2019-11-27 |
Model Number | VT585U |
Catalog Number | VT585U |
Lot Number | 027853 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | JOHNSON & JOHNSON SURGICAL VISION, INC. |
Manufacturer Address | 1700 E ST ANDREW PLACE SANTA ANA CA 92705 US 92705 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-27 |