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TPLC
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show TPLC since
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Device
tubing/tubing with filter, insufflation, laparoscopic
Product Code
NKC
Regulation Number
884.1730
Device Class
1
MDR Year
MDR Reports
MDR Events
2015
11
11
2016
2
2
2018
1
1
2019
3
3
2020
3
3
2021
2
2
2022
2
2
2023
4
4
2024
4
4
Device Problems
MDRs with this Device Problem
Events in those MDRs
Infusion or Flow Problem
8
8
Device Operates Differently Than Expected
5
5
Kinked
3
3
No Flow
3
3
Leak/Splash
2
2
Break
2
2
Output Problem
2
2
Manufacturing, Packaging or Shipping Problem
2
2
Gas/Air Leak
2
2
Obstruction of Flow
2
2
Connection Problem
2
2
Inaccurate Flow Rate
2
2
Temperature Problem
2
2
Device Contaminated During Manufacture or Shipping
1
1
Compatibility Problem
1
1
Mechanical Problem
1
1
Complete Blockage
1
1
Therapeutic or Diagnostic Output Failure
1
1
Failure to Align
1
1
Material Distortion
1
1
Improper Flow or Infusion
1
1
Material Separation
1
1
Labelling, Instructions for Use or Training Problem
1
1
Detachment of Device or Device Component
1
1
Loss of or Failure to Bond
1
1
No Device Output
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Known Impact Or Consequence To Patient
9
9
No Clinical Signs, Symptoms or Conditions
7
7
No Consequences Or Impact To Patient
6
6
Myocarditis
2
2
Burn(s)
2
2
No Patient Involvement
2
2
Discomfort
2
2
No Code Available
1
1
Insufficient Information
1
1
Bradycardia
1
1
Unspecified Respiratory Problem
1
1
Therapeutic Effects, Unexpected
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
DeRoyal Industries Inc
II
Aug-28-2013
2
Karl Storz Endoscopy
III
May-09-2020
3
Karl Storz Endoscopy
II
Nov-16-2017
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