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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 Code
OCX
Regulation Number
876.1500
Device Class
2
Premarket Reviews
Manufacturer
Decision
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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