MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 05,07 report with the FDA on 2004-08-13 for OPHTHALAS 532 EYELITE manufactured by Alcon - Irvine Technology Center.
[20760081]
Reporter noted laser became inoperable during case; treatment with laser discontinued. Completed case doing a buckle. Prognosis reported as good. Cancelled remaining cases for the day.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 2028159-2004-00191 |
MDR Report Key | 538964 |
Report Source | 05,07 |
Date Received | 2004-08-13 |
Date of Report | 2004-07-15 |
Date of Event | 2004-07-15 |
Date Mfgr Received | 2004-07-15 |
Date Added to Maude | 2004-08-17 |
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 | 0 |
Manufacturer Contact | CHARLES DOLBEE |
Manufacturer Street | 6201 SOUTH FREEWAY |
Manufacturer City | FORT WORTH TX 761342099 |
Manufacturer Country | US |
Manufacturer Postal | 761342099 |
Manufacturer Phone | 8175518317 |
Manufacturer G1 | ALCON - IRVINE TECHNOLOGY CENTER |
Manufacturer Street | 15800 ALTON PARKWAY |
Manufacturer City | IRVINE CA 92618 |
Manufacturer Country | US |
Manufacturer Postal Code | 92618 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | OPHTHALAS 532 EYELITE |
Generic Name | LASER PHOTOCOAGULATOR |
Product Code | HQB |
Date Received | 2004-08-13 |
Model Number | 532 EYELITE |
Catalog Number | 532 EYELITE |
Lot Number | NA |
ID Number | NA |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Implant Flag | N |
Date Removed | A |
Device Sequence No | 1 |
Device Event Key | 528249 |
Manufacturer | ALCON - IRVINE TECHNOLOGY CENTER |
Manufacturer Address | 15800 ALTON PKWY. IRVINE CA 92618 US |
Baseline Brand Name | OPHTHALAS 532 EYELITE |
Baseline Generic Name | LASER PHOTOCOAGULATOR |
Baseline Model No | 532 EYELITE |
Baseline Catalog No | 532 EYELITE |
Baseline ID | NA |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2004-08-13 |