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TPLC
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show TPLC since
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2024
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Device
clamp
Product Code
HXD
Regulation Number
878.4800
Device Class
1
MDR Year
MDR Reports
MDR Events
2019
125
125
2020
114
114
2021
75
75
2022
88
88
2023
99
99
2024
39
39
Device Problems
MDRs with this Device Problem
Events in those MDRs
Device-Device Incompatibility
251
251
Break
129
129
Mechanical Jam
55
55
Structural Problem
39
39
Naturally Worn
34
34
Physical Resistance/Sticking
20
20
Mechanical Problem
18
18
Detachment of Device or Device Component
16
16
Material Twisted/Bent
16
16
Component Missing
15
15
Crack
15
15
Difficult to Open or Close
13
13
Material Deformation
12
12
Fracture
11
11
Unintended Movement
9
9
Appropriate Term/Code Not Available
7
7
Material Integrity Problem
6
6
Fitting Problem
6
6
Device Slipped
4
4
Illegible Information
4
4
Use of Device Problem
3
3
Entrapment of Device
3
3
Positioning Failure
2
2
Difficult to Remove
2
2
Connection Problem
2
2
Separation Problem
2
2
Adverse Event Without Identified Device or Use Problem
2
2
Positioning Problem
2
2
Scratched Material
2
2
No Apparent Adverse Event
1
1
Insufficient Flow or Under Infusion
1
1
Device Damaged Prior to Use
1
1
Contamination /Decontamination Problem
1
1
Material Disintegration
1
1
Fluid/Blood Leak
1
1
Loose or Intermittent Connection
1
1
Incorrect Measurement
1
1
Patient Problems
MDRs with this Patient Problem
Events in those MDRs
No Clinical Signs, Symptoms or Conditions
290
290
No Consequences Or Impact To Patient
200
200
No Code Available
27
27
Insufficient Information
20
20
Not Applicable
14
14
No Known Impact Or Consequence To Patient
5
5
Patient Problem/Medical Problem
3
3
No Patient Involvement
3
3
Hemorrhage/Bleeding
3
3
Hyperglycemia
1
1
Failure of Implant
1
1
Foreign Body In Patient
1
1
Device Embedded In Tissue or Plaque
1
1
Skin Inflammation/ Irritation
1
1
Recalls
Manufacturer
Recall Class
Date Posted
1
MEDLINE INDUSTRIES, LP - Northfield
II
Mar-29-2024
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