background image

Page 22 

 3101126 Rev A Vapotherm Oxygen Assist Module Instructions for Use    

Section 19   Specifications

Masimo SET

®

 Accuracy Specifications

 

Saturation (% SpO

2

) – During No Motion Conditions1

 

  Adults, Pediatrics 

70% - 100% ± 2 

digits 

   

 

   

0% - 69% unspecified

 

  Neonates 

70% - 100% ± 3 digits

 

   

0% - 69% unspecified

 

Saturation (% SpO

2

) – During No Motion Conditions2,3

 

  Adults, Pediatrics 

70% - 100% ± 3 digits

 

   

0% - 69% unspecified

 

  Neonates 

70% - 100% ± 3 digits

 

   

0% - 69% unspecified

 

Pulse Rate (bpm) – During No Motion Conditions1

 

  Adults, Pediatric, Neonates 

25 to 240 ± 3 digits

 

Pulse Rate (bpm) – During Motion Conditions2,3

 

  Adults, Pediatric, Neonates 

25 to 240 ± 5 digits

1 The Masimo SET technology with Masimo sensors has been validated for no motion accuracy in human blood studies on 

healthy adult male and female volunteers with light to dark skin pigmentation in induced hypoxia studies in the range of 70-

100% SpO

2

 against a laboratory CO-Oximeter and ECG monitor. This variation equals ±1standard deviation. Plus or minus one 

standard deviation encompasses 68% of the population.

2 The Masimo SET technology with Masimo sensors has been validated for motion accuracy in human blood studies on healthy 

adult male and female volunteers with light to dark skin pigmentation in induced hypoxia studies while performing rubbing and 

tapping motions, at 2 to 4 Hz at an amplitude of 1 to 2 cm and a non-repetitive motion between 1 to 5 Hz at an amplitude of 2 to 3 

cm in induced hypoxia studies in the range of 70-100% SpO

2

 against a laboratory CO-Oximeter and ECG monitor. This variation 

equals ±1 standard deviation, which encompasses

3 The Masimo SET technology has been validated for low perfusion accuracy in bench top testing against a Biotek Index 2™ 

simulator and Masimo’s simulator with signal strengths of greater than 0.02% and transmission of greater than 5% for saturations 

ranging from 70 to 100%. This variation equals ±1 standard deviation. Plus or minus one standard deviation encompasses 68% 

of the population.

4 The Masimo SET Technology with Masimo Neo sensors has been validated for neonatal motion accuracy in human blood 

studies on healthy adult male and female volunteers with light to dark skin pigmentation in induced hypoxia studies while 

performing rubbing and tapping motions, at 2 to 4 Hz at an amplitude of 1 to 2 cm and a non-repetitive motion between 1 to 5 

Hz at an amplitude of 2 to 3 cm in induced hypoxia studies in the range of 70-100% SpO

2

 against a laboratory CO-Oximeter 

and ECG monitor. This variation equals ±1 standard deviation. Plus or minus one standard deviation encompasses 68% of the 

population. 1% has been added to the results to account for the effects of fetal hemoglobin present in neonates.

5 The Masimo SET technology with Masimo sensors has been validated for pulse rate accuracy for the range of 25 -240 bpm in 

bench top testing against a Biotek Index 2™ simulator. This variation equals ±1 standard deviation. Plus or minus one standard 

deviation encompasses 68% of the population.

6 See sensor directions for use (DFU) for complete application information. Unless otherwise indicated, reposition reusable 

sensors at least every 4 hours and adhesive sensors at least every 8 hours.

11 Sensor accuracy specified when used with Masimo technology using a Masimo patient cable for LNOP sensors, RD SET 

sensors, the LNCS sensors, or the M-LNCS sensors. Numbers represent Arms (RMS error compared to the reference). Because 

pulse oximeter measurements are statistically distributed, only about two-thirds of the measurements can be expected to fall 

within a range of ± Arms compared to the reference value. Unless otherwise noted, SpO

2

 accuracy is specified from 70% to 

100%. Pulse Rate accuracy is specified from 25 to 240 bpm.

12 Masimo M-LNCS, LNOP, RD SET, and LNCS sensors types have the same optical and electrical properties and may differ 

only in application type (adhesive/non-adhesive/hook & loop), cable lengths, optical component locations (top or bottom of sensor 

as aligned with cable), adhesive material type/size, and connector type (LNOP 8 pin modular plug, RD 15 pin modular plug, 

LNCS 9 pin, cable based, and M-LNCS 15 pin, cable based). All sensor accuracy information and sensor application instructions 

are provided with the associated sensor directions for use.

References

For Vapotherm Precision Flow specifications, see the Precision Flow Instructions for Use.
For SpO

2

 sensor specification, see the documentation provided with the sensor.

Summary of Contents for Oxygen Assist Module

Page 1: ...Oxygen Assist Module for use with Vapotherm Precision Flow Instructions for Use...

Page 2: ...ection 7 Patient Admission 12 Section 8 Alarm Setup 13 Section 9 SpO2 Setup 13 Section 10 O2 Setup 16 Section 11 System Shutdown 17 Section 12 Graphical Trend Display 17 Section 13 Logging of Variable...

Page 3: ...osed as an unsorted municipal waste and must be collected separately Please contact an authorized representative of the manufacturer for information concerning the decommissioning of your equipment De...

Page 4: ...y Therapy Equipment and Guidelines for Prevention of Nosocomial Pneumonia For more information see the Precision Flow Instructions for Use General Warnings Federal Law U S restricts the use of this de...

Page 5: ...rous oxide To ensure safety avoid stacking multiple devices or placing anything on the device during operation To protect against injury follow the directions below Avoid placing the device on surface...

Page 6: ...lly calibrated in healthy adult volunteers with normal levels of carboxyhemoglobin COHb and methemoglobin MetHb Do not adjust repair open disassemble or modify the Oxygen Assist Module or accessories...

Page 7: ...her use Injury to personnel could occur Disposal of product Comply with local laws in the disposal of the device and or its accessories To minimize radio interference other electrical equipment that e...

Page 8: ...sis of real time measurements and trending to choose the appropriate O2 delivery The use of smart averaging and hysteresis algorithms by the Masimo SET SpO2 monitor protects the system from artifacts...

Page 9: ...ssist Module and provides 12VDC to the Oxygen Assist Module Contact Vapotherm if you believe your power adapter to not be functional or you need a replacement Only use power adapter as provided by Vap...

Page 10: ...w s interface port 6 Plug the Oxygen Assist Module Power Supply into the Oxygen Assist Module and into an electrical outlet marked Hospital Grade or Hospital Only NOTE Ensure proper orientation on Pow...

Page 11: ...oxygen Using Menus To call up a menu press the desired menu tab Alternately parameter boxes will redirect to the associated menu Notes Unless otherwise stated the change to settings takes effect when...

Page 12: ...tely place the Oxygen Assist Module in Manual O2 Mode A manual change in O2 on the Precision Flow with 120 90 60 30 15 5 seconds selected will suppress Auto Mode O2 titration for that period of time b...

Page 13: ...rm is generated stating No Sensor Connected Alarm messages cycle in the message area For a list of alarm messages and required action please see the section Alarm and Status Messages For alarm indicat...

Page 14: ...ors may cause incorrect SpO2 readings Before using the sensor carefully read the sensor documentation including all warnings cautions and instructions The accuracy of pulse oximetry readings can be ad...

Page 15: ...es Signal IQ values of less than 0 3 The SpO2 display range is from 1 100 A value of indicates that no measurement is available The pulse rate display range is from 1 240 bpm A value of indicates that...

Page 16: ...trol knob Note See description of Fallback O2 Functionality on the following page for more information 3 Insert Oxygen Assist Module Time Card and Press Start Case When the patient is stable press the...

Page 17: ...s If the Oxygen Assist Module has exited the Auto mode check the patient sensor placement connections and settings When clinically indicated place the Oxygen Assist Module back into Auto mode in the P...

Page 18: ...ng and disinfecting instructions for the SpO2 sensor and patient cable see the instructions provided with the sensor Section 14 Cleaning and Disinfecting Section 17 Referenced Documentation Precision...

Page 19: ...Clinical patient condition Check patient Sensor not connected Check sensor and cable connections Sensor off patient Check sensor application Sensor or cables damaged Check sensor and cables Replace i...

Page 20: ...yperbaric cond Storage and Shipping Ambient Temperature 10 50 C Ambient Relative Humidity 20 90 RH Contact with Patient Indirectly via SpO2 sensor and Precision Flow O2 cannula Liquid Ingress Protecti...

Page 21: ...trical Equipment Part 1 6 General requirements for basic safety and essential performance Collateral Standard Usability IEC 60601 1 8 2006 Second Edition Am 1 2012 for use in conjunction with IEC 6060...

Page 22: ...female volunteers with light to dark skin pigmentation in induced hypoxia studies while performing rubbing and tapping motions at 2 to 4 Hz at an amplitude of 1 to 2 cm and a non repetitive motion bet...

Page 23: ...Case Check SpO2 Defective Cable Replace cable enter MANUAL Mode or End Case Check SpO2 Defective Sensor Replace sensor enter MANUAL Mode or End Case Check SpO2 Incompatible Adhesive Sensor Replace se...

Page 24: ...Demo Mode Reconnect sensor with good signal Check SpO2 Interference Detected Reconnect sensor with good signal Check SpO2 Low Perfusion Index Reconnect sensor with good signal Check SpO2 Low Signal I...

Page 25: ...target and sets the FiO2 delivery rate accordingly The algorithm makes near immediate adjustments within 10 seconds to changes in SpO2 readings learns from past changes and anticipates short term cha...

Page 26: ...s declaration electromagnetic emissions The Oxygen Assist Module is intended for use in the electromagnetic environment specified below The customer or the user of the Oxygen Assist Module should ass...

Page 27: ...y should be that of a typical commercial or hospital environment Surge IEC 61000 4 5 0 5 1 and 2 kV Line s to Ground 1 kV line s to Line s 0 5 1 and 2 kV 1 kV Mains power quality should be that of a t...

Page 28: ...paration distance in meters m Field strengths from fixed RF transmitters as determined by an electromagnetic site surveya should be less than the compliance level in each frequency range b Interferenc...

Page 29: ...ed maximum output power of transmitter W Separation distance according to frequency of transmitter m 50 kHz to 80 MHz outside ISM bands d 1 2 P 150 kHz to 80 MHz in ISM bands d 1 2 P 800 MHz to 2 5 GH...

Page 30: ...Page 30 3101126 Rev A Vapotherm Oxygen Assist Module Instructions for Use This Page Intentionally Blank...

Page 31: ...3101126 Rev A Vapotherm Oxygen Assist Module Instructions for Use Page 31 This Page Intentionally Blank...

Page 32: ...for Use Vapotherm Inc 100 Domain Drive Exeter NH 03833 USA Phone 603 658 0011 Fax 603 658 0181 RMS UK Limited 28 Trinity Road Nailsea North Somerset BS48 4NU United Kingdom Phone 44 1275 85 88 91 Fax...

Reviews: