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U.S. Department of Health and Human Services

TPLC - Total Product Life Cycle

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Device endoscopic irrigation/suction system
Definition To supply sterile water, other solutions and/or suction to endoscopes during endoscopic procedures.
Product CodeOCX
Regulation Number 876.1500
Device Class 2


Premarket Reviews
ManufacturerDecision
BIOTEX INC.
  SUBSTANTIALLY EQUIVALENT 1
BIOTEX, INC.
  SUBSTANTIALLY EQUIVALENT 1
CHANGZHOU ENDOCLEAN MEDICAL DEVICE CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
CHONGQING JINSHAN SCIENCE & TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
CIPHER SURGICAL LIMITED
  SUBSTANTIALLY EQUIVALENT 1
DIVERSATEK HEALTHCARE
  SUBSTANTIALLY EQUIVALENT 1
ERBE USA, INC.
  SUBSTANTIALLY EQUIVALENT 1
FINEMEDIX CO., LTD.
  SUBSTANTIALLY EQUIVALENT 2
GA HEALTH COMPANY LIMITED
  SUBSTANTIALLY EQUIVALENT 6
HOBBS MEDICAL, INC.
  SUBSTANTIALLY EQUIVALENT 1
KEYMED (MEDICAL AND INDUSTRIAL EQUIPMENT) LTD.
  SUBSTANTIALLY EQUIVALENT 1
MEDIVATORS
  SUBSTANTIALLY EQUIVALENT 1
NISSHA MEDICAL TECHNOLOGIES SAS
  SUBSTANTIALLY EQUIVALENT 1
OLYMPUS MEDICAL SYSTEMS CORPORATION
  SUBSTANTIALLY EQUIVALENT 1
SANESO, INC.
  SUBSTANTIALLY EQUIVALENT 1
YANGZHOU FARTLEY MEDICAL INSTRUMENT TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 1
ZHEJIANG CHUANGXIANG MEDICAL TECHNOLOGY CO., LTD.
  SUBSTANTIALLY EQUIVALENT 2

MDR Year MDR Reports MDR Events
2020 11 11
2021 8 8
2022 18 18
2023 52 52
2024 21 21

Device Problems MDRs with this Device Problem Events in those MDRs
Leak/Splash 69 69
Material Fragmentation 7 7
Detachment of Device or Device Component 6 6
Fluid/Blood Leak 5 5
Break 4 4
Positioning Problem 4 4
Adverse Event Without Identified Device or Use Problem 4 4
Device-Device Incompatibility 2 2
Suction Failure 2 2
Defective Device 2 2
Material Twisted/Bent 2 2
Device Handling Problem 2 2
Increase in Pressure 2 2
Gas Output Problem 2 2
Incomplete or Inadequate Connection 1 1
Collapse 1 1
Insufficient Information 1 1
Wrong Label 1 1
Manufacturing, Packaging or Shipping Problem 1 1
Contamination /Decontamination Problem 1 1
Backflow 1 1
Use of Device Problem 1 1
Difficult or Delayed Activation 1 1
Optical Problem 1 1
Free or Unrestricted Flow 1 1
Activation Failure 1 1
Nonstandard Device 1 1

Patient Problems MDRs with this Patient Problem Events in those MDRs
No Clinical Signs, Symptoms or Conditions 89 89
No Consequences Or Impact To Patient 6 6
Insufficient Information 5 5
No Known Impact Or Consequence To Patient 3 3
Foreign Body In Patient 2 2
Hemorrhage/Bleeding 2 2
Gastrointestinal Hemorrhage 1 1
Hematoma 1 1
Keratitis 1 1
Obstruction/Occlusion 1 1
Thrombosis/Thrombus 1 1
Bruise/Contusion 1 1

Recalls
Manufacturer Recall Class Date Posted
1 GA HEALTH COMPANY LIMITED II Dec-18-2020
2 Hobbs Medical, Inc. II Oct-07-2022
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