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TPLC
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show TPLC since
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2024
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Device
device, surgical, cryogenic
Product Code
GXH
Regulation Number
882.4250
Device Class
2
Premarket Reviews
Manufacturer
Decision
ATRICURE INC.
SUBSTANTIALLY EQUIVALENT
1
ATRICURE, INC.
SUBSTANTIALLY EQUIVALENT
4
MYOSCIENCE INC
SUBSTANTIALLY EQUIVALENT
5
MYOSCIENCE, INC
SUBSTANTIALLY EQUIVALENT
3
PACIRA BIOSCIENCES, INC.
SUBSTANTIALLY EQUIVALENT
1
PACIRA PHARMACEUTICALS INC.
SUBSTANTIALLY EQUIVALENT
1
MDR Year
MDR Reports
MDR Events
2015
1
1
2016
1
1
2017
2
2
2018
14
14
2019
6
6
2020
4
4
2021
6
6
2022
3
3
2023
4
4
2024
2
2
Device Problems
MDRs with this Device Problem
Events in those MDRs
Adverse Event Without Identified Device or Use Problem
16
16
Tear, Rip or Hole in Device Packaging
7
7
Temperature Problem
4
4
Use of Device Problem
3
3
Output Problem
2
2
Device Dislodged or Dislocated
2
2
Break
1
1
Crack
1
1
Energy Output Problem
1
1
Gas/Air Leak
1
1
Moisture or Humidity Problem
1
1
Device Handling Problem
1
1
Unexpected Therapeutic Results
1
1
Human-Device Interface Problem
1
1
Insufficient Cooling
1
1
Fluid/Blood Leak
1
1
Scratched Material
1
1
Detachment of Device or Device Component
1
1
No Apparent Adverse Event
1
1
Material Separation
1
1
Activation Failure
1
1
Inappropriate/Inadequate Shock/Stimulation
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Patient Involvement
8
8
No Clinical Signs, Symptoms or Conditions
5
5
Cryogenic Burn
5
5
Nerve Damage
4
4
Inadequate Pain Relief
3
3
Pneumothorax
2
2
No Known Impact Or Consequence To Patient
2
2
Burn(s)
2
2
Pain
2
2
Arrhythmia
1
1
Hypersensitivity/Allergic reaction
1
1
Decreased Sensitivity
1
1
Electric Shock
1
1
Perforation of Esophagus
1
1
No Information
1
1
Perforation
1
1
Burn, Thermal
1
1
Injury
1
1
Visual Impairment
1
1
Partial thickness (Second Degree) Burn
1
1
Respiratory Insufficiency
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
Myoscience Inc
II
Jul-22-2015
2
Myoscience Inc
II
Jul-20-2013
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