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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device stethoscope, manual
Product CodeLDE
Regulation Number 870.1875
Device Class 1

MDR Year MDR Reports MDR Events
2017 1 1
2018 1 1
2019 3 3
2020 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Adverse Event Without Identified Device or Use Problem 2 2
Appropriate Term/Code Not Available 1 1
Defective Component 1 1
Device Issue 1 1
Patient-Device Incompatibility 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Irritation 2 2
Skin Irritation 2 2
Reaction 1 1
No Code Available 1 1
Rash 1 1
Abrasion 1 1
Hearing Impairment 1 1
Inflammation 1 1

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