TISSUE SLEEVE FOR POLY DRIVER 2020-00-410 202000410

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-01-03 for TISSUE SLEEVE FOR POLY DRIVER 2020-00-410 202000410 manufactured by Medos International Sàrl Ch.

MAUDE Entry Details

Report Number1526439-2020-00151
MDR Report Key9547330
Report SourceCOMPANY REPRESENTATIVE
Date Received2020-01-03
Date of Report2019-12-06
Date of Event2019-12-03
Date Mfgr Received2020-01-30
Device Manufacturer Date2019-08-19
Date Added to Maude2020-01-03
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 ContactKARA DITTY-BOVARD
Manufacturer StreetCHEMIN-BLANC 38
Manufacturer CityLE LOCLE 02400
Manufacturer CountrySZ
Manufacturer Postal02400
Manufacturer Phone6103142063
Manufacturer G1DEPUY SPINE INC
Manufacturer Street325 PARAMOUNT DRIVE
Manufacturer CityRAYNHAM MA 02767
Manufacturer CountryUS
Manufacturer Postal Code02767
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameTISSUE SLEEVE FOR POLY DRIVER
Generic NameCANNULA, SURGICAL, GENERAL & PLASTIC SURGERY
Product CodeGEA
Date Received2020-01-03
Returned To Mfg2019-12-18
Model Number2020-00-410
Catalog Number202000410
Lot NumberPC4710467
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerMEDOS INTERNATIONAL SàRL CH
Manufacturer AddressCHEMIN-BLANC 38 LE LOCLE 02400 SZ 02400


Patients

Patient NumberTreatmentOutcomeDate
10 2020-01-03

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