MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a user facility report with the FDA on 2020-03-05 for AUTO LOGIC PXB001DAR manufactured by Arjohuntleigh, A Branch Of Arjo Ltd Med Ab.
Report Number | 3005619970-2020-00003 |
MDR Report Key | 9791819 |
Report Source | USER FACILITY |
Date Received | 2020-03-05 |
Date of Report | 2020-03-05 |
Date of Event | 2020-02-03 |
Date Mfgr Received | 2020-02-19 |
Date Added to Maude | 2020-03-05 |
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 | KINGA STOLINSKA |
Manufacturer Street | KS. WAWRZYNIAKA 2 |
Manufacturer City | KOMORNIKI 62-052 |
Manufacturer Country | PL |
Manufacturer Postal | 62-052 |
Manufacturer Phone | 688282467 |
Manufacturer G1 | ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB |
Manufacturer Street | ARJOHUNTLEIGH HOUSE, HOUGHTON HALL BUSINESS PARK |
Manufacturer City | HOUGHTON REGIS, BEDFORDSHIRE LU5 5XF |
Manufacturer Country | UK |
Manufacturer Postal Code | LU5 5XF |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | AUTO LOGIC |
Generic Name | MATTRESS, AIR FLOTATION, ALTERNATING PRESSURE |
Product Code | FNM |
Date Received | 2020-03-05 |
Model Number | PXB001DAR |
Device Availability | * |
Device Eval'ed by Mfgr | * |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ARJOHUNTLEIGH, A BRANCH OF ARJO LTD MED AB |
Manufacturer Address | ARJOHUNTLEIGH HOUSE, HOUGHTON HALL BUSINESS PARK HOUGHTON REGIS, BEDFORDSHIRE LU5 5XF UK LU5 5XF |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-05 |