• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

New Search show TPLC since Back to Search Results
Device bilirubin (total and unbound) in the neonate test system
Product CodeMQM
Regulation Number 862.1113
Device Class 1

MDR Year MDR Reports MDR Events
2019 6 6
2020 1 1
2021 1 1
2023 14 14
2024 3 3

Device Problems MDRs with this Device Problem Events in those MDRs
Low Readings 12 12
Unexpected Therapeutic Results 2 2
Low Test Results 2 2
False Negative Result 2 2
Patient Data Problem 2 2
Fitting Problem 1 1
Insufficient Information 1 1
Output Problem 1 1
Defective Component 1 1
High Readings 1 1
Non Reproducible Results 1 1
No Apparent Adverse Event 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
Jaundice 12 12
No Clinical Signs, Symptoms or Conditions 7 7
No Known Impact Or Consequence To Patient 4 4
Test Result 1 1
No Consequences Or Impact To Patient 1 1

-
-