MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a foreign,health professional,u report with the FDA on 2019-10-02 for LIPIFLOW ACTIVATOR II LFD-2000 220150 manufactured by Johnson & Johnson Surgical Vision, Inc..
Report Number | 3008169506-2019-00007 |
MDR Report Key | 9146259 |
Report Source | FOREIGN,HEALTH PROFESSIONAL,U |
Date Received | 2019-10-02 |
Date of Report | 2019-10-02 |
Date of Event | 2019-08-29 |
Report Date | 2005-01-01 |
Date Reported to FDA | 2005-01-01 |
Date Reported to Mfgr | 2005-01-10 |
Date Mfgr Received | 2019-09-05 |
Device Manufacturer Date | 2019-05-13 |
Date Added to Maude | 2019-10-02 |
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 | 6830 MEADOWRIDGE COURT |
Manufacturer City | ALPHARETTA GA 30005 |
Manufacturer Country | US |
Manufacturer Postal Code | 30005 |
Single Use | 0 |
Previous Use Code | 0 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | LIPIFLOW ACTIVATOR II |
Generic Name | LIPIFLOW |
Product Code | ORZ |
Date Received | 2019-10-02 |
Model Number | LFD-2000 |
Catalog Number | 220150 |
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 | 1. Required No Informationntervention | 2019-10-02 |