MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-11 for CITADEL BED FRAME CX811A3F3AMAB0 manufactured by Arjohuntleigh Polska Sp. Z O.o..
Report Number | 3007420694-2020-00058 |
MDR Report Key | 9817265 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-11 |
Date of Report | 2020-03-11 |
Date of Event | 2020-02-11 |
Date Mfgr Received | 2020-02-11 |
Device Manufacturer Date | 2017-04-10 |
Date Added to Maude | 2020-03-11 |
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 POLSKA SP. Z O.O. |
Manufacturer Street | UL. KS. PIOTRA WAWRZYNIAKA 2 |
Manufacturer City | KOMORNIKI PL-62052 |
Manufacturer Country | PL |
Manufacturer Postal Code | PL-62052 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | CITADEL BED FRAME |
Generic Name | BED, AC-POWERED ADJUSTABLE HOSPITAL |
Product Code | FNL |
Date Received | 2020-03-11 |
Model Number | CX811A3F3AMAB0 |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | Y |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ARJOHUNTLEIGH POLSKA SP. Z O.O. |
Manufacturer Address | UL. KS. PIOTRA WAWRZYNIAKA 2 KOMORNIKI PL-62052 PL PL-62052 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2020-03-11 |