MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other,use report with the FDA on 2019-11-01 for ELEKTA INFINITY manufactured by Elekta Ltd.
Report Number | 9617016-2019-00007 |
MDR Report Key | 9266185 |
Report Source | HEALTH PROFESSIONAL,OTHER,USE |
Date Received | 2019-11-01 |
Date of Report | 2019-11-01 |
Date Mfgr Received | 2019-10-04 |
Date Added to Maude | 2019-11-01 |
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 |
Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | PMS |
Manufacturer Street | LINAC HOUSE FLEMING WAY |
Manufacturer City | CRAWLEY, WEST SUSSEX RH109RR |
Manufacturer Country | UK |
Manufacturer Postal | RH10 9RR |
Manufacturer G1 | ELEKTA LTD |
Manufacturer Street | LINAC HOUSE FLEMING WAY |
Manufacturer City | CRAWLEY, RH109RR |
Manufacturer Country | UK |
Manufacturer Postal Code | RH10 9RR |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ELEKTA INFINITY |
Generic Name | ACCELERATOR, LINEAR, MEDICAL |
Product Code | IYE |
Date Received | 2019-11-01 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ELEKTA LTD |
Manufacturer Address | LINAC HOUSE FLEMING WAY CRAWLEY, RH109RR UK RH10 9RR |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 2019-11-01 |