Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • 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 trap, sterile specimen
Regulation Description Vacuum-powered body fluid suction apparatus.
Product CodeBYZ
Regulation Number 880.6740
Device Class 2

MDR Year MDR Reports MDR Events
2020 1 1
2021 1 1
2022 2 2
2023 4 4
2024 1 1
2025 1 1

Device Problems MDRs with this Device Problem Events in those MDRs
Leak/Splash 2 2
Product Quality Problem 2 2
Disconnection 1 1
Device Contaminated During Manufacture or Shipping 1 1
Entrapment of Device 1 1
Suction Failure 1 1
Material Integrity Problem 1 1
Component Missing 1 1
Particulates 1 1
Suction Problem 1 1
Connection Problem 1 1
Loose or Intermittent Connection 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 3 3
Insufficient Information 3 3
Appropriate Clinical Signs, Symptoms, Conditions Term / Code Not Available 2 2
Foreign Body Sensation in Eye 1 1
Muscle Weakness 1 1
Bradycardia 1 1
Respiratory Insufficiency 1 1
Airway Obstruction 1 1

-
-