CONF INTRO NDLE, DIA, 11G 6" 283903611

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 2019-11-11 for CONF INTRO NDLE, DIA, 11G 6" 283903611 manufactured by Medos International Sàrl Ch.

MAUDE Entry Details

Report Number1526439-2019-52379
MDR Report Key9305512
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2019-11-11
Date of Report2019-09-04
Date of Event2019-09-04
Date Mfgr Received2019-11-07
Date Added to Maude2019-11-11
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 G1MEDOS INT SPINE
Manufacturer StreetCHEMIN BLANC 38
Manufacturer CityLE LOCLE
Manufacturer CountrySZ
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameCONF INTRO NDLE, DIA, 11G 6"
Generic NameNEEDLE, ASPIRATION AND INJECTION, DISPOSABLE
Product CodeGAA
Date Received2019-11-11
Returned To Mfg2019-11-07
Model Number283903611
Catalog Number283903611
Lot Number237306
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 2019-11-11

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