inforMED
MalfunctionIXL

DIAGNOST 76

Received Jul 7, 2011

Report 3003768251-2011-00041 · MDR key 2182213

Device

Product problems

  • Break

Patient

Not reported

  • No Information

Narrative

Additional Manufacturer Narrative

THE INVESTIGATION IS CURRENTLY ONGOING AND CONCLUSIONS WILL BE SENT IN A FOLLOW UP REPORT TO THE FDA. (B)(4).

Description of Event or Problem

THE CUSTOMER REPORTED THAT THE CABLE HOLDER WAS BROKEN.