AIR PEN DRIVE 05.001.080

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 2020-02-25 for AIR PEN DRIVE 05.001.080 manufactured by Depuy Synthes Products Llc.

MAUDE Entry Details

Report Number8030965-2020-01265
MDR Report Key9752810
Report SourceCOMPANY REPRESENTATIVE,FOREIG
Date Received2020-02-25
Date of Report2020-02-12
Date of Event2020-01-01
Date Mfgr Received2020-03-28
Device Manufacturer Date2017-01-25
Date Added to Maude2020-02-25
Event Key0
Report Source CodeManufacturer report
Manufacturer LinkY
Number of Patients in Event0
Adverse Event Flag3
Product Problem Flag3
Reprocessed and Reused Flag3
Health Professional3
Initial Report to FDA3
Report to FDA3
Event Location3
Manufacturer ContactMS. KARA DITTY-BOVARD
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF 4436
Manufacturer CountrySZ
Manufacturer Postal4436
Manufacturer Phone6103142063
Manufacturer G1OBERDORF SYNTHES PRODUKTIONS GMBH
Manufacturer StreetEIMATTSTRASSE 3
Manufacturer CityOBERDORF 4436
Manufacturer CountrySZ
Manufacturer Postal Code4436
Single Use3
Previous Use Code3
Event Type3
Type of Report3

Device Details

Brand NameAIR PEN DRIVE
Generic NameMOTOR, DRILL, PNEUMATIC
Product CodeHBB
Date Received2020-02-25
Returned To Mfg2020-03-25
Catalog Number05.001.080
OperatorHEALTH PROFESSIONAL
Device AvailabilityR
Device AgeDA
Device Eval'ed by MfgrY
Device Sequence No1
Device Event Key0
ManufacturerDEPUY SYNTHES PRODUCTS LLC
Manufacturer AddressEIMATTSTRASSE 3 OBERDORF 4436 SZ 4436


Patients

Patient NumberTreatmentOutcomeDate
10 2020-02-25

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