• 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 dna probe, trichomonas vaginalis
Product CodeMJK
Regulation Number 866.2660
Device Class 1

MDR Year MDR Reports MDR Events
2022 1 1
2023 6 6
2024 2 2

Device Problems MDRs with this Device Problem Events in those MDRs
Unable to Obtain Readings 3 3
Use of Device Problem 2 2
Failure of Device to Self-Test 2 2
Appropriate Term/Code Not Available 1 1
High impedance 1 1
Failure to Power Up 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 8 8
Burn(s) 1 1

-
-