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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device enteral syringes with enteral specific connectors
Definition Delivers nutrition, medication, or hydration orally or to a gastrointestinal tube or extension set using AAMI/CN3(PS):2014 compliant connectors.
Product CodePNR
Regulation Number 876.5980
Device Class 2


Premarket Reviews
ManufacturerDecision
AMSINO INTERNATIONAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
ANHUI TIANKANG MEDICAL TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
CAIR LG
  SUBSTANTIALLY EQUIVALENT 1
COVIDIEN
  SUBSTANTIALLY EQUIVALENT 4
INTERNATIONAL MEDICAL INDUSTRIES, INC.
  SUBSTANTIALLY EQUIVALENT 1
INTERVENE GROUP LIMITED
  SUBSTANTIALLY EQUIVALENT 1
JIANGSU CAINA MEDICAL CO., LTD.
  SUBSTANTIALLY EQUIVALENT 3
JIANGSU KANGBAO MEDICAL EQUIPMENT CO., LTD
  SUBSTANTIALLY EQUIVALENT 1
JIANGSU MICSAFE MEDICAL TECHNOLOGY CO., LTD
  SUBSTANTIALLY EQUIVALENT 1
JIANGSU SHENLI MEDICAL PRODUCTION CO., LTD
  SUBSTANTIALLY EQUIVALENT 1
JIANGYIN CAINA TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
MEDELA, INC.
  SUBSTANTIALLY EQUIVALENT 1
MEDLINE INDUSTRIES, INC.
  SUBSTANTIALLY EQUIVALENT 1
NEOMED, INC.
  SUBSTANTIALLY EQUIVALENT 4
NINGBO TIANYI MEDICAL APPLIANCE CO., LTD.
  SUBSTANTIALLY EQUIVALENT 2
PENTAFERTE ITALIA S.R.L.
  SUBSTANTIALLY EQUIVALENT 2
SHANGHAI KINDLY ENTERPRISE DEVELOPMENT GROUP CO., LTD
  SUBSTANTIALLY EQUIVALENT 1
SHANTOU WEALY MEDICAL INSTRUMENT CO., LTD.
  SUBSTANTIALLY EQUIVALENT 2
SHINVA ANDE HEALTHCARE APPARATUS CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
U&U MEDICAL TECHNOLOGY CO.,LTD
  SUBSTANTIALLY EQUIVALENT 1
VR MEDICAL TECHNOLOGY
  SUBSTANTIALLY EQUIVALENT 1

MDR Year MDR Reports MDR Events
2016 1 1
2017 3 3
2018 2 2
2019 8 8
2020 2 2
2021 5 5
2022 2 2
2023 11 11
2024 3 3

Device Problems MDRs with this Device Problem Events in those MDRs
Device Markings/Labelling Problem 5 5
Fluid/Blood Leak 4 4
Break 4 4
Product Quality Problem 3 3
Device Contamination with Chemical or Other Material 3 3
Volume Accuracy Problem 2 2
Defective Device 2 2
Entrapment of Device 2 2
Excess Flow or Over-Infusion 2 2
Manufacturing, Packaging or Shipping Problem 2 2
Connection Problem 2 2
Measurement System Incompatibility 1 1
Mechanical Jam 1 1
No Flow 1 1
Adverse Event Without Identified Device or Use Problem 1 1
Patient Device Interaction Problem 1 1
Physical Resistance/Sticking 1 1
Fail-Safe Did Not Operate 1 1
Air/Gas in Device 1 1
Incorrect Measurement 1 1
Mechanical Problem 1 1
Device Difficult to Setup or Prepare 1 1
Fail-Safe Design Failure 1 1
Detachment Of Device Component 1 1
Crack 1 1
Patient-Device Incompatibility 1 1
Gas/Air Leak 1 1
Difficult to Remove 1 1
Inadequacy of Device Shape and/or Size 1 1
Imprecision 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Known Impact Or Consequence To Patient 11 11
No Clinical Signs, Symptoms or Conditions 11 11
Insufficient Information 9 9
No Consequences Or Impact To Patient 2 2
No Patient Involvement 1 1
No Information 1 1
Increased Intra-Peritoneal Volume (IIPV) 1 1
Abscess 1 1
Adhesion(s) 1 1
Aspiration/Inhalation 1 1
Death 1 1

Recalls
Manufacturer Recall Class Date Posted
1 Cardinal Health 200, LLC I Feb-02-2024
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