MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional report with the FDA on 2018-11-07 for FIXTURE BIOHELIX 23X80 -12 1811 manufactured by Integrum Ab.
        [126445888]
Fixture loosening. No deviation in batch documentation. According to report form the cause of failure is unknown. No further investigation.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 3011386779-2018-00012 | 
| MDR Report Key | 8048127 | 
| Report Source | HEALTH PROFESSIONAL | 
| Date Received | 2018-11-07 | 
| Date of Report | 2018-11-06 | 
| Date of Event | 2018-06-19 | 
| Date Facility Aware | 2018-06-19 | 
| Report Date | 2018-07-17 | 
| Date Reported to Mfgr | 2018-07-17 | 
| Date Mfgr Received | 2018-07-17 | 
| Date Added to Maude | 2018-11-07 | 
| 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 | MR. NIKLAS HOFVERBERG | 
| Manufacturer Street | KROKSL | 
| Manufacturer City | MOLNDAL, MOLNDAL, VASTRA GOTALAND | 
| Manufacturer G1 | INTEGRUM AB | 
| Manufacturer Street | KROKSLATTS FABRIKER 50 | 
| Manufacturer City | MOLNDAL, VASTRA GOTALAND 43137 | 
| Manufacturer Country | SW | 
| Manufacturer Postal Code | 43137 | 
| Single Use | 3 | 
| Remedial Action | PM | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 3 | 
| Brand Name | FIXTURE BIOHELIX 23X80 -12 | 
| Generic Name | FIXTURE BIOHELIX 23X80 -12 | 
| Product Code | PJY | 
| Date Received | 2018-11-07 | 
| Model Number | 1811 | 
| Catalog Number | 1811 | 
| Lot Number | P266262 | 
| Operator | LAY USER/PATIENT | 
| Device Availability | N | 
| Device Age | 17 MO | 
| Device Eval'ed by Mfgr | N | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | INTEGRUM AB | 
| Manufacturer Address | KROKSLATTS FABRIKER 50 MOLNDAL, VASTRA GOTALAND 43137 SW 43137 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2018-11-07 |