SPIR HA MULTIHOLES CUP D52 100050252

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2020-03-30 for SPIR HA MULTIHOLES CUP D52 100050252 manufactured by Depuy France Sas - 3003895575.

MAUDE Entry Details

Report Number1818910-2020-09624
MDR Report Key9900355
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-03-30
Date of Report2020-03-12
Date of Event2020-01-01
Date Mfgr Received2020-03-12
Device Manufacturer Date2013-12-20
Date Added to Maude2020-03-30
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 ContactMS. KARA DITTY-BOVARD
Manufacturer Street7 ALLEE IRENE JOLIOT-CURIE B.P. 256
Manufacturer CitySAINT PRIEST CEDEX 69801
Manufacturer CountryFR
Manufacturer Postal69801
Manufacturer Phone6107428552
Manufacturer G1LEEDS MFG & MATERIAL WAREHOUSE
Manufacturer StreetST ANTHONYS ROAD
Manufacturer CityLEEDS LS118DT
Manufacturer CountryUK
Manufacturer Postal CodeLS11 8DT
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameSPIR HA MULTIHOLES CUP D52
Generic NameSPIROFIT IMPLANTS : HIP METAL ACETABULAR CUPS
Product CodeLPH
Date Received2020-03-30
Catalog Number100050252
Lot Number5219153
OperatorHEALTH PROFESSIONAL
Device AvailabilityN
Device Eval'ed by MfgrR
Device Sequence No1
Device Event Key0
ManufacturerDEPUY FRANCE SAS - 3003895575
Manufacturer Address7 ALLEE IRENE JOLIOT-CURIE B.P. 256 SAINT PRIEST CEDEX 69801 FR 69801


Patients

Patient NumberTreatmentOutcomeDate
101. Required No Informationntervention 2020-03-30

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.