KD906 Kappa 900 D
Implantable Pulse Generator (IPG)
KD906 Kappa 900 D
Information

Device Survival Probability

KD901_KD903_KD906_KDR901_KDR903_KDR906_SURV
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    1 yr 2 yr 3 yr 4 yr 5 yr 6 yr 7 yr 8 yr 9 yr 10 yr at 125.0 mo                    
% Excluding Normal Battery Depletion 100.0 100.0 100.0 100.0 100.0 100.0 99.9 99.9 99.9 99.9 99.9                    
% Including Normal Battery Depletion 99.5 99.3 99.0 98.4 97.4 95.0 85.9 59.9 27.5 7.3 2.0                    
#   109129 99802 90749 82082 73618 65173 53726 33247 12731 2554 519                    
  • Including Normal Battery Depletion – This curve includes devices that have reached at least 80% of expected longevity. This curve is most representative of clinical performance and how long the device will last.
  • Excluding Normal Battery Depletion – This is the malfunction free survival curve.
Information

Advisories For This Model

  • There are no advisories for this model.

Performance Notes For This Model

Information

Product Characteristics

Generator Type IPG
NBD Code DDD
Max. Delivered Energy N/A
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Connector Style 5/6mm UNI
Serial Number Prefix PLD
Mass 28.5 g
Volume 14.2 cc
Waveform N/A
X-Ray ID PLD
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5/6mm UNI
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Estimated Longevity

Amplitude Setting 500 Lead Ω 1000 Lead Ω
Low 2.5 V (A, RV) 7.7 8.6
Nominal 3.5 V (A, RV) 6.3 7.7
High 5.0 V (A, RV) 4.4 6.0
Footnote

Longevity estimates based on the following device usage. Pace/Sense Mode DDD ; Atrial Pulse Width 0.4 ms; Right Ventricle Pulse Width 0.4 ms; Lower Pace Rate 60 bpm; Right Ventricle Percent Paced 100 %; Upper Sensing Rate 130 ppm; Atrial Percent Paced 100 %; Atrial Fib Percent of Time 0 %Hide this content

Information

EOL Indication

From the point that the ERI is set, the pacemaker will operate at ERI conditions for approximately three months for typical pacemaker configurations during the normal operating life.

Information

Distribution Data

US Market Release2002-01-09
CE Approval Date2001-09-28
Registered USA Implants
Estimated Active USA Implants
Normal Battery Depletions
US Market Release2002-01-09
CE Approval Date2001-09-28
Estimated WW Distribution133
Normal Battery Depletions4
Information

Malfunctions (USA)

Therapy Function Not Compromised
Therapy Function Compromised
Information

Malfunctions (WW)

Therapy Function Not Compromised
Therapy Function Compromised
Information

Elective Replacement (ERI)

Replacement message on programmer. Nonmagnet mode VVI 65 ppm Magnet mode VOO 65 ppm

Data as of February 3, 2017

www.medtronic.com/productperformance 476050