• 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 device, occlusion, umbilical
Product CodeFOD
Regulation Number 880.5950
Device Class 1

MDR Year MDR Reports MDR Events
2018 4 4
2019 1 1
2020 1 1
2021 2 2
2022 4 4

Device Problems MDRs with this Device Problem Events in those MDRs
Product Quality Problem 3 3
Detachment of Device or Device Component 3 3
Mechanical Problem 2 2
Appropriate Term/Code Not Available 2 2
Device Dislodged or Dislocated 1 1
Unintended Movement 1 1
Insufficient Information 1 1
Device Slipped 1 1
Break 1 1
Detachment Of Device Component 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 4 4
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Hemorrhage/Bleeding 2 2
Blood Loss 2 2
No Code Available 1 1
Seizures 1 1
No Consequences Or Impact To Patient 1 1
Foreign Body Reaction 1 1

-
-