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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle
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Device goniometer, nonpowered
Product CodeKQW
Regulation Number 888.1520
Device Class 1

MDR Year MDR Reports MDR Events
2018 1 1
2022 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
Disconnection 1 1
Mechanical Problem 1 1
Device-Device Incompatibility 1 1
Mechanical Jam 1 1
Unintended Movement 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 2 2
No Known Impact Or Consequence To Patient 1 1

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