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TPLC
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Device
cuff, tracheal tube, inflatable
Regulation Description
Inflatable tracheal tube cuff.
Product Code
BSK
Regulation Number
868.5750
Device Class
2
Premarket Reviews
Manufacturer
Decision
AW TECHNOLOGIES APS
SUBSTANTIALLY EQUIVALENT
1
COVIDIEN, LLC
SUBSTANTIALLY EQUIVALENT
1
HOSPITECH RESPIRATION , LTD.
SUBSTANTIALLY EQUIVALENT
1
IDMED
SUBSTANTIALLY EQUIVALENT
1
SHANGHAI LONGMANN TECH CO., LTD.
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2021
9
18
2022
4
4
2023
51
52
2024
133
134
2025
46
46
2026
3
3
Device Problems
MDRs with this Device Problem
Events in those MDRs
Gas/Air Leak
132
141
Unable to Obtain Readings
33
33
Loose or Intermittent Connection
20
20
Break
18
18
Electrical /Electronic Property Problem
12
12
Insufficient Information
9
9
Pressure Problem
4
13
No Audible Alarm
3
3
Charging Problem
3
3
Display or Visual Feedback Problem
3
3
Mechanical Jam
3
3
Component Missing
2
2
Infusion or Flow Problem
2
2
Gas Output Problem
2
2
No Device Output
2
2
Failure to Read Input Signal
1
1
Material Split, Cut or Torn
1
1
Mechanical Problem
1
1
Incomplete or Inadequate Connection
1
1
Crack
1
1
Unintended Deflation
1
1
Smoking
1
1
Failure to Zero
1
2
Defective Component
1
1
Positioning Problem
1
1
Deflation Problem
1
1
Inadequate Instructions for Healthcare Professional
1
1
Battery Problem
1
1
Use of Device Problem
1
1
Inflation Problem
1
1
Material Deformation
1
1
Device Emits Odor
1
1
Product Quality Problem
1
10
Installation-Related Problem
1
2
Fracture
1
1
Appropriate Term/Code Not Available
1
1
Human-Device Interface Problem
1
10
No Flow
1
1
Fluid/Blood Leak
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
235
237
Insufficient Information
6
6
Cardiac Arrest
2
11
Hypoxia
2
11
Bronchospasm
1
1
Respiratory Insufficiency
1
1
Ventilator Dependent
1
10
Unintended Extubation
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Covidien
II
Sep-29-2023
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