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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: MEDOS INTERNATIONAL SàRL CH UNKNOWN SCREWS SCREW,FIXATION,BONE

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MEDOS INTERNATIONAL SàRL CH UNKNOWN SCREWS SCREW,FIXATION,BONE Back to Search Results
Device Problem Unintended Movement
Event Type  Injury  
Search Alerts/Recalls

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Brand NameUNKNOWN SCREWS
Type of DeviceSCREW,FIXATION,BONE
Manufacturer (Section D)
MEDOS INTERNATIONAL SàRL CH
chemin-blanc 38
le locle 02400
SZ  02400
Manufacturer (Section G)
MEDOS INT SPINE
chemin blanc 38
le locle 02400
SZ  02400
Manufacturer Contact
kara ditty-bovard
chemin-blanc 38
le locle  02400
  02400
6103142063
MDR Report Key9612875
Report Number1526439-2020-00417
Device Sequence Number1
Product CodeHWC
Report Source Manufacturer
Source Type COMPANY REPRESENTATIVE,FOREIG
Reporter Occupation OTHER HEALTH CARE PROFESSIONAL
Type of Report Initial,Followup
Report Date 01/08/2020
1 Device Was Involved in the Event
1 Patient Was Involved in the Event
Date FDA Received01/21/2020
Is This An Adverse Event Report? Yes
Is This A Product Problem Report? Yes
Device Operator HEALTH PROFESSIONAL
Was Device Available For Evaluation? No
Is The Reporter A Health Professional? Yes
Was the Report Sent to FDA?
Event Location No Information
Date Manufacturer Received02/18/2020
Was Device Evaluated By Manufacturer? Device Not Returned To Manufacturer
Is The Device Single Use? Yes
Is this a Reprocessed and Reused Single-Use Device?
Type of Device Usage Unkown

Patient TREATMENT DATA
Date Received: 01/21/2020 Patient Sequence Number: 1
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