Reprocessed sensors may not meet the needs of patients in challenging conditions when an accurate and timely pulse oximetry reading is needed the most.


Nellcor™ remanufactured sensors

Remanufactured like new. Reliable every time.

100%

of Nellcor ™ remanufactured sensors

 Restored to factory settings and comparable to brand-new sensors

 Met the same process and performance requirements as brand new sensors

 Are only remanufactured one time to ensure quality


Do you know the difference?

Third-party reprocessed sensors

Sensor reprocessing by third parties varies across reprocessors according to their limited product knowledge and the set target performance level.
 

 Not affiliated with or supported by Medtronic

 No knowledge of Nellcor™ proprietary manufacturing procedures

 Reprocessing of a single sensor may be performed multiple times; in this case, performance levels might not be comparable to new devices

Nellcor™ remanufactured sensors

In the Medtronic remanufacturing process, a sensor is assembled the same way as a new sensor. Optical testing is used to confirm sensors meet quality and calibration specications.§
 

 Deep knowledge of the Nellcor™ products and their manufacturing processes§

 Designed to provide sensors equivalent to new terms of compliance to original product specifcations§,1

 Each used sensor meeting the criteria for remanufacturing goes through 50 proprietary procedures and specification checks and can only be remanufactured once, to ensure performance is not affected.§

Stryker reprocessed sensors

do not offer the same functionality and usability
as Nellcor™ remanufactured


Stryker™* reprocessed sensors do not offer the same functionality and usability as Nellcor™ remanufactured sensors.

Stryker out-of-the-box
failures: up to 10%


Stryker™* reprocessed sensors do not offer the same functionality and usability as Nellcor™ remanufactured sensors.

Stryker visual inspection
failures: up to 20%


Stryker™* reprocessed sensors do not offer the same functionality and usability as Nellcor™ remanufactured sensors.

Stryker optical failure
rate:
up to 1.96%


Stryker™* reprocessed sensors do not offer the same functionality and usability as Nellcor™ remanufactured sensors.

Stryker optical signal strength:
weaker by up to 37%

Nellcor™ remanufactured sensors

meet original performance and quality specifications. They are 100% like-new and have 0% impact on workflow.


Nellcor™ remanufactured sensors meet original performance and quality specifications, are 100% like new, and have 0% impact on workflow.

Nellcor™ out-of-the-box
 failures: 0%


Nellcor™ remanufactured sensors meet original performance and quality specifications, are 100% like new, and have 0% impact on workflow.

Nellcor™ visual inspection
 failures: 0%


Nellcor™ remanufactured sensors meet original performance and quality specifications, are 100% like new, and have 0% impact on workflow.

Nellcor™ optical failure rate:
 up to 0.35%


Nellcor™ remanufactured sensors meet original performance and quality specifications, are 100% like new, and have 0% impact on workflow.

Nellcor™ optical signal
 strength: 100%


Key takeaway

At the visual inspection rate seen in this analysis, a hospital would have to purchase up to 20% more Stryker sensors to compensate for quality issues.

Stryker reprocessed sensors may not meet the needs in challenging conditions when an accurate and timely pulse oximetry reading is needed the most.


Sensor adherence and accuracy

A stronger peel force is problematic for neonatal, frail, and compromised patients as this may lead to discomfort and skin damage.


A stronger peel force is problematic for neonatal, frail, and compromised patients as this may lead to discomfort and skin damage.

A stronger peel force is problematic for neonatal, frail, and compromised patients as this may lead to discomfort and skin damage.

Extra layers on several reprocessed sensors require more force to bend, which can lead to poor sensor adherence.

A stronger peel force is problematic for neonatal, frail, and compromised patients as this may lead to discomfort and skin damage.


An extra bandage layer can cause greater thickness between optical components adversely affecting signal strength, resulting in more dropouts and alarms.

  Peeling force Bending force Thickness
Stryker A compared to MAXAR No significant difference 49.5% more force 0.85 mm thicker
Stryker N compared to MAXNR 49% stronger 26.4% more force 0.23 mm thicker

Key takeaway

Stryker reprocessed sensors were found to be less agile, less flexible, and less likely to conform to the application site, which may result in poor performance — more dropouts, more alarms, and reduced sensor life — and could lead to more waste.



To learn more about Nellcor™ pulse oximetry