FIXTURE BIOHELIX 23X80 -12 1811

MAUDE Adverse Event Report

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.

Event Text Entries

[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


MAUDE Entry Details

Report Number3011386779-2018-00012
MDR Report Key8048127
Report SourceHEALTH PROFESSIONAL
Date Received2018-11-07
Date of Report2018-11-06
Date of Event2018-06-19
Date Facility Aware2018-06-19
Report Date2018-07-17
Date Reported to Mfgr2018-07-17
Date Mfgr Received2018-07-17
Date Added to Maude2018-11-07
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Reporter OccupationOTHER HEALTH CARE PROFESSIONAL
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMR. NIKLAS HOFVERBERG
Manufacturer StreetKROKSL
Manufacturer CityMOLNDAL, MOLNDAL, VASTRA GOTALAND
Manufacturer G1INTEGRUM AB
Manufacturer StreetKROKSLATTS FABRIKER 50
Manufacturer CityMOLNDAL, VASTRA GOTALAND 43137
Manufacturer CountrySW
Manufacturer Postal Code43137
Single Use3
Remedial ActionPM
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameFIXTURE BIOHELIX 23X80 -12
Generic NameFIXTURE BIOHELIX 23X80 -12
Product CodePJY
Date Received2018-11-07
Model Number1811
Catalog Number1811
Lot NumberP266262
OperatorLAY USER/PATIENT
Device AvailabilityN
Device Age17 MO
Device Eval'ed by MfgrN
Device Sequence No1
Device Event Key0
ManufacturerINTEGRUM AB
Manufacturer AddressKROKSLATTS FABRIKER 50 MOLNDAL, VASTRA GOTALAND 43137 SW 43137


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2018-11-07

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.