BiPAP rental and medical equipment rental cost in Bangalore
If you need a bipap rental, look no further we are here to help you with the best rates. Call us for medical equipment rental and bipap rental, avoids losing value since medical equipment have low resale value & high depreciation. Enjoy an easy therapy experience with a rented BiPAP, knowing a technician is always available for support. We are the right medical equipment suppliers in Bangalore to choose from.
BiPAP rental for all modes per month Rs 4500 with humidifier
Auto BiPAP machine Rs 4000
Invasive trachea ventilation rent Rs 8000 per month
Accessories: BiPAP mask & Hose pipe
Medical equipment rental type BiPAP
Modes: S, ST, T, V & Auto.
Brands: ResMed, Philips, Nisco med
Accessories: NIV Mask Vented & Hose
BiPAP filter for ResMed
Medical equipment suppliers rent 3500 Rs rent per month.
Medical equipment type CPAP
Modes: Auto & APAP
Brands: ResMed, Philips, Nisco med
Accessories: NIV Mask Vented & Hose
CPAP filter for ResMed
Medical equipment suppliers rent: 3000 Rs rent per month
Why BiPAP machine for rent is a good choice?
Renting a BiPAP machine is the best choice for short-term recovery. Many patients won’t need a BiPAP machine after recovery, so renting is cost-effective. For example, a one-month rental is only Rs 3500, much less than the Rs 85000 cost of buying.
ISO-Certified Equipment Maintenance: Our rental machines adhere to ISO standards, ensuring top-notch BiPAP machine rent in Bangalore.
Rigorous Disinfection Protocols: Rest easy knowing our machines are thoroughly disinfected for your safety.
Cutting-Edge BiPAP Rentals: Access the latest BiPAP machines available for rent.
Patient-Centric Support: Phone and video call support to help patients.
Data Retrieval Assistance: We help you retrieve vital data post-usage for better monitoring.
Local Language Support: Communicate comfortably in Kannada, Tamil, Telugu, Hindi, or Malayalam.
Affordable Rates: BiPAP machine rent starts from just 100 Rs per day.
Comprehensive Respiratory Care: We give end-to-end respiratory care solutions.
What is a BiPAP, Bi level machine?
BiPAP machines come in various types, each offering different modes to cater to specific patient needs.
The most common modes include ST, S, V, SV, and Auto. For instance, the ST (Spontaneous/Timed) mode is often recommended for patients with lung issues.
This mode delivers breaths both spontaneously and at timed intervals, ensuring adequate ventilation. However, it will not be suitable for everyone, so it should only be used based on medical advice.
On the other hand, the S (Spontaneous) mode provides mandatory breaths if the patient’s breathing pauses due to obstructive sleep apnea (OSA) or central sleep apnea (CSA), helping in maintaining proper ventilation.
Moreover, the V (Volume) mode is designed to deliver a set volume of air per breath, ensuring that the patient receives the correct amount of air.
In contrast, the Auto BiPAP mode adjusts breath delivery within a preset range, based on the patient’s needs. To achieve optimal performance and comfort, using the right mask and accessories is crucial.
For long-term users, it is advisable to select masks, hoses, and machines from the same brand.
This choice ensures a proper fit and effective pressure delivery. Masks are available in Small, Medium, and Large sizes, which are based on the nasal bridge rather than face size.
Additionally, they are categorized as Full Face Masks, Nasal Masks, and Nasal Pillow Masks, allowing for customization based on individual needs and preferences.
Changing the modes on a BiPAP machine is not straightforward; it requires entering the clinical menu to adjust settings.
You can access this menu by pressing and holding two buttons together. On most machines, you press and hold down the HOME and Volume keys together for 12 seconds to enter the clinical menu.
Once inside, you’ll find options to switch between modes ST, S, V, AVAPS, AUTO, and CPAP, among others. Additionally, you can control the humidification settings here. For instance, you can adjust the heat delivered by the humidifier from 0 to 7 on most models.
The clinical menu allows to set the ramp settings, which control how pressure increases over a chosen period.
The most important settings in a clinical menu is IPAP (Inspiratory Positive Airway Pressure) and EPAP (Expiratory Positive Airway Pressure). IPAP determines the pressure the machine provides when you inhale, while EPAP controls the pressure maintained during exhalation.
By understanding and configuring these settings, you can significantly enhance the effectiveness and comfort of your BiPAP therapy.
Types of BiPAP
Resmed 10VAuto & S
Units: cm H2O and hPa (1 cm H2O = 0.98 hPa)
Power Supply:
90W power supply unit
AC input: 100–240V, 50–60Hz, 1.0–1.5A, Class II
Aircraft input: 115V, 400Hz, 1.5A, Class II (nominal)
DC output: 24V, 3.75A
Typical power consumption: 53W (57VA)
Peak power consumption: 104W (108VA)
Environmental Conditions
Operating temperature: +5°C to +35°C
Device air flow can be higher than room temperature.
Remains safe up to 40°C ambient temperature.
Operating humidity: 10 to 95% relative humidity, non-condensing
Operating altitude: Sea level to 2,591 m (air pressure range: 1013 hPa to 738 hPa)
Storage/Transport Temperature: -20°C to +60°C
Storage/Transport humidity: 5 to 95% relative humidity, non-condensing
Electromagnetic Compatibility
Complies with IEC 60601-1-2:2014 for residential, commercial, and light industry environments.
Keep mobile communication devices at least 1 m away from the device.
Classification:
EN60601-1:2006/A1:2013, Class II (double insulation), Type BF, Ingress protection IP22.
Sensors
Internal, 0 to 40 cm H2O (0 to 40 hPa), analog gauge pressure type.
Pressure sensor:
Flow sensor:
Internal, -70 to +180 L/min, digital mass flow type.
Safety Features
Device shuts down if steady pressure exceeds:
30 cm H2O (30 hPa) for more than 6 seconds.
40 cm H2O (40 hPa) for more than 1 second.
Sound Levels
SlimLine tubing:
Pressure: 25 dBA (± 2 dBA uncertainty)
Power: 33 dBA (± 2 dBA uncertainty)
Standard tubing:
Pressure: 25 dBA (± 2 dBA uncertainty)
Power: 33 dBA (± 2 dBA uncertainty)
With humidification:
Pressure: 27 dBA (± 2 dBA uncertainty)
Power: 35 dBA (± 2 dBA uncertainty)
Physical Attributes (Device and Humidifier)
Dimensions: 116 mm (H) x 255 mm (W) x 150 mm (D)
Weight: 1248 g (with cleanable humidifier)
Air outlet: 22 mm (ISO 5356-1:2015 compliant)
Housing: Flame-retardant engineering thermoplastic
Water capacity: 380 mL (maximum fill line)
Humidifier material: Injection-molded plastic, stainless steel, silicone seal
Temperature Settings
Maximum heater plate temperature: 68°C
Cut-out temperature: 74°C
Maximum gas temperature: ≤ 41°C
Air Filter
Standard filter: Polyester non-woven fiber, >75% efficiency for ~7 micron dust
Hypoallergenic filter: Acrylic and polypropylene fibers, >98% efficiency for ~7-8 micron dust, >80% efficiency for ~0.5 micron dust
Aircraft Use
Complies with FAA requirements (RTCA/DO-160, section 21, category M) for air travel.
Wireless Module
Technology used: 4G, 3G, 2G
Device should be at least 2 cm from the body during operation (except for masks, tubes, or accessories).
Displayed Values (Resolution & Range)
Mask pressure: 2–25 cm H2O (2–25 hPa), resolution 0.1 cm H2O
Flow-derived values:
Leak: 0–120 L/min, resolution 1 L/min
Tidal volume: 0–4000 mL, resolution 1 mL
Respiratory rate: 0–50 BPM, resolution 1 BPM
Minute ventilation: 0–30 L/min, resolution 0.1 L/min
Ti: 0.1–4.0 sec, resolution 0.1 sec
I:E ratio: 1:100 – 2:1, resolution 0.1
Value Accuracy
Pressure measurement: Mask pressure ±[0.5 cm H2O (0.5 hPa) + 4% of measured value]
Flow and flow-derived values:
Flow: ±6 L/min or 10% of reading (whichever is greater) for 0 to 150 L/min
Leak: ±12 L/min or 20% of reading (whichever is greater) for 0 to 60 L/min
Tidal volume: ±20%
Respiratory rate: ±1.0 BPM
Minute ventilation: ±20%
Measurement System Uncertainties (ISO 80601-2-70:2015)
Time: ±10 ms
Flow: ±1.5 L/min or ±2.7% of reading
Volume (< 100 mL): ±5 mL or 6% of reading
Volume (≥ 100 mL): ±20 mL or 3% of reading
Static pressure: ±0.15 cm H2O (hPa)
Dynamic pressure: ±0.27 cm H2O (hPa)
Remed Lumis S & ST (VAPS)
Power Supply
90W unit
AC input range: 100–240V, 50–60Hz, 1.0–1.5A, Class II
AC input for aircraft use: 115V, 400Hz, 1.5A, Class II
DC output: 24V, 3.75A
Typical power usage: 53W (57VA)
Peak power consumption: 104W (108VA)
Pressure Sensor at Air Outlet
Mask pressure: 2–25 cm H2O (2–25 hPa)
Display resolution: 0.1 cm H2O (0.1 hPa)
Flow-Derived Values
Leak: 0–120 L/min, resolution: 1 L/min
Tidal volume: 0–4000 mL, resolution: 1 mL
Respiratory rate: 0–50 breaths per minute (BPM), resolution: 1 BPM
Minute ventilation: 0–30 L/min, resolution: 0.1 L/min
Inspiratory time (Ti): 0.1–4.0 sec, resolution: 0.1 sec
I:E ratio (inspiration/expiration): 1:100 to 2:1, resolution: 0.1
Measurement Accuracy
Mask pressure: ±[0.5 cm H2O (0.5 hPa) + 4% of measured value]
Flow: ±6 L/min or 10% of reading, whichever is greater, at 0 to 150 L/min
Leak: ±12 L/min or 20% of reading, 0–60 L/min
Tidal volume: ±20%
Respiratory rate: ±1 BPM
Minute ventilation: ±20%
Results expressed at STPD (Standard Temperature and Pressure, Dry)
Measurement System Uncertainties (per ISO 80601-2-70:2015)
Flow measures: ±1.5 L/min or ±2.7%
Volume (<100 mL): ±5 mL or 6%
Volume (≥100 mL): ±20 mL or 3%
Pressure measures: ±0.15 cm H2O (0.15 hPa)
Time measures: ±10 milliseconds
Pressure Accuracy
Maximum static variation at 10 cm H2O: ±0.5 cm H2O
Consistent with or without humidification
Environmental Conditions
Operating temperature: +5°C to +35°C
Operating humidity: 10% to 95% relative humidity, non-condensing
Operating altitude: Sea level to 8,500 feet (2,591 m)
Storage temperature: -20°C to +60°C
Storage humidity: 5% to 95% relative humidity, non-condensing
Electromagnetic Compatibility
Compliant with IEC 60601-1-2:2014 standards
Recommended to keep mobile communication devices at least 1 m away
Classification (per EN60601-1:2006/A1:2013)
Class II (double insulation), Type BF
Ingress protection rating: IP22
Sensors
Pressure sensor: Internally located at outlet, 0–40 cm H2O range
Flow sensor: Located at inlet, -70 to +180 L/min range
Sound Levels (per ISO 80601-2-70:2015)
SlimLine air tubing: 25 dBA (±2 dBA)
Standard tubing: 25 dBA (±2 dBA)
With humidification: 27 dBA (±2 dBA)
Physical Dimensions
Device with humidifier: 116 mm (H) x 255 mm (W) x 150 mm (D)
Weight: 1268 g (device and humidifier)
Water Reservoir
Maximum fill line: 380 mL
Filters
Standard: Polyester non-woven fibre, 75% arrestance for ~7-micron dust
Hypoallergenic: Acrylic and polypropylene fibres, 98% efficiency for ~7-8 micron dust
Aircraft Compliance
Meets FAA requirements for air travel
Wireless Module
Technology: 2G, 3G, 4G (LTE)
Pressure Accuracy for Bilevel Modes
Inspiratory and expiratory pressure accuracy varies based on breath rates and tubing type (Standard or SlimLine)
Flow and Compliance Characteristics
Resistance and compliance of tubing vary based on flow and tubing type (Standard, SlimLine, ClimateLineAir)
Philips Dream station BiPAP
Specifications:
Environmental:
Operating Temperature: 5° to 35° C (41° to 95° F)
Storage Temperature: -20° to 60° C (-4° to 140° F)
Relative Humidity (operating & storage): 15 to 95% (non-condensing)
Atmospheric Pressure: 101 to 77 kPa (0 – 2286 m / 0 – 7500 ft)
Physical:
Dimensions: 15.7 x 19.3 x 8.4 cm (6.2” L x 7.6” W x 3.3” H)
Weight (Device with power supply): Approximately 1.33 kg (2.94 lbs)
Service Life:
The expected service life of the DreamStation Therapy Device and Link Module is 5 years.
Standards Compliance:
IEC 60601-1: General Requirements for Basic Safety and Essential Performance of Medical Electrical Equipment
ISO 80601-2-70: Sleep Apnea Breathing Therapy Equipment
ISO 80601-2-74: Medical Electrical Equipment – Part 2-74: Particular Requirements for Basic Safety and Essential Performance of respiratory humidifying equipment
EN 60601-1-2: Electromagnetic Compatibility
RTCA/DO-160G section 21, category M: Emission of Radio Frequency Energy
IEC 60601-1 Classification:
Type of Protection Against Electric Shock: Class II Equipment
Degree of Protection Against Electric Shock: Type BF Applied Part
Degree of Protection Against Ingress of Water: IP22 (Device, Link Module, and 80W power supply are drip-proof)
Mode of Operation: Continuous
Electrical:
AC Power Consumption (with 80W power supply): 100 – 240 VAC, 50/60 Hz, 2.0-1.0 A
DC Power Consumption: 12 VDC, 6.67 A
Fuses: No user-replaceable fuses
Radio Specifications:
Operating Frequency Range: 2402 – 2480 MHz
Maximum Output Power: <10 dBm
Modulation: GFSK, P/4 DQPSK, 8DQPSK
Intake Port Filters:
Pollen Filter: 100% Polyester, 88% Efficient @ 7-10 micron size
Ultra-fine Filter: Blended Synthetic Fiber, 95% Efficient @ 0.5-0.7 micron size
Declared Dual-Number Noise Emissions Values (ISO 4871):
A-weighted sound pressure level:
Device: 27 dB(A) with an uncertainty of 2 dB
Device with Humidifier: 29 dB(A) with an uncertainty of 2 dB
A-weighted sound power level:
Device: 35 dB(A) with an uncertainty of 2 dB
Device with Humidifier: 37 dB(A) with an uncertainty of 2 dB
Noise test code as per ISO 80601-2-70:2015, ISO 3744, and ISO 4871
Pressure Accuracy:
Pressure Increments: 4.0 to 20.0 cm H2O (in 0.5 cm H2O increments)
Maximum static pressure accuracy (ISO 80601-2-70:2015):
10 cm H2O ± 0.5 cm H2O (± 1.0 cm H2O with 12 mm standard tubes)
Measurement uncertainty: 3.7%
Dynamic Pressure Accuracy:
Maximum dynamic pressure variation (ISO 80601-2-70:2015):
Pressure (10 BPM, 15 BPM, 20 BPM):
<10 cm H2O: ± 0.4, ± 0.5, ± 0.8 cm H2O
≥10.0 to 20 cm H2O: ± 0.5, ± 0.8, ± 1.0 cm H2O
Measurement uncertainty: 4.3%
Maximum Flow Rate (typical):
Test pressures (cm H2O):
4.0 | 8.0 | 12.0 | 16.0 | 20.0
22 mm tubing:
Measured pressure at the patient connection port (cm H2O): 3.7 | 7.7 | 11.2 | 14.9 | 18.9
Average flow at the patient connection port (l/min): 85 | 124 | 131 | 132 | 128
15 mm tubing (heated or non-heated):
Measured pressure at the patient connection port (cm H2O): 3.7 | 7.4 | 10.9 | 14.9 | 18.8
Average flow at the patient connection port (l/min): 86 | 127 | 134 | 133 | 117
12 mm tubing:
Measured pressure at the patient connection port (cm H2O): 4.0 | 7.0 | 11.0 | 15.0 | 19.0
Average flow at the patient connection port (l/min): 85 | 95 | 94 | 100 | 102
Tubing Specifications:
12 mm performance tubing (PR12):
Tubing resistance: @30 l/min: 0.03 hPa/l/min (cm H2O/l/min)
Tubing compliance (@ 60 hPa): 0.44 ml/hPa (ml/cm H2O)
15 mm performance tubing (PR15):
Tubing resistance: @15 l/min: 0.006 hPa/l/min | @30 l/min: 0.01 hPa/l/min
Tubing compliance (@ 60 hPa): 0.52 ml/hPa (ml/cm H2O)
22 mm performance tubing:
Tubing resistance: @15 l/min: 0.00 hPa/l/min | @30 l/min: 0.003 hPa/l/min
Tubing compliance (@ 60 hPa): 0.73 ml/hPa (ml/cm H2O)
Cleaning and Disinfection Guidelines
WARNINGS!
Regular cleaning of the device and its accessories is crucial to prevent respiratory infections.
Always unplug the device before cleaning to avoid electric shock.
Use mild, non-toxic soap for cleaning.
Follow manufacturer instructions for cleaning the mask and tubing, including the frequency of cleaning.
Ensure the device is disconnected from power, and the water chamber and heating plate have cooled to room temperature to avoid burns.
Do not open or modify the device, as there are no user-serviceable parts inside. Only authorized service agents should perform repairs.
Never service or maintain the device while it’s in use by a patient.
CAUTIONS!
Overheating may shorten the lifespan of materials.
Avoid using cleaning solutions containing chlorinated lime, chlorine, or aromatic agents, as they may harden materials or reduce their lifespan. Do not use soaps containing moisturizing agents or antimicrobials.
Avoid cleaning or drying the device and its accessories in temperatures above 80°C (176°F) as this will reduce product life.
Never immerse the device in any fluids.
1. Cleaning the Mask and Headgear
Refer to the user manual for specific mask cleaning instructions.
2. Cleaning the SpO2 Kit
Refer to the user manual for instructions on cleaning the SpO2 Kit.
3. Cleaning the Water Chamber
Open the water chamber as illustrated.
Clean the water chamber with a soft cloth that will not scratch it. If needed, dip the cloth in mild soap, then rinse thoroughly and wipe dry.
Follow instructions to reassemble the water chamber.
WARNINGS!
Daily emptying and cleaning of the water chamber helps prevent mold and bacteria growth.
Allow the water chamber to cool before removing it from the device.
CAUTIONS!
Ensure the water chamber is completely cool before cleaning. Avoid letting water enter the device.
Rinse thoroughly after cleaning to prevent soap residue buildup, then wipe it dry with a lint-free cloth.
Inspect the water chamber regularly for leaks or damage. Replace if necessary.
Daily cleaning of the water chamber is recommended.
Cleaning the Transfer Box
Remove the water chamber first, then remove the transfer box.
Rinse the transfer box with clean water or clean it with a soft cloth. Rinse thoroughly and dry with a soft cloth.
Reinstall the transfer box.
CAUTION!
Clean the transfer box weekly.
5. Cleaning the Device Enclosure
Wipe the device’s surface with a soft, slightly damp cloth.
CAUTIONS!
Ensure the enclosure is dry before using the device again to prevent moisture from entering.
Clean the enclosure weekly.
Cleaning the Tubing
Remove the tubing from both the device and mask.
Clean the tubing with warm water and a mild detergent, then rinse thoroughly.
Air-dry the tubing in a cool, well-ventilated area, avoiding direct sunlight. Ensure the tubing is completely dry before reuse.
CAUTION!
Clean the tubing weekly.
Replacing the Air Filter / PM2.5 Filter
Attach the air filter to the filter cap and install it in the device.
Replace the air filter with the PM2.5 filter as needed.
CAUTIONS!
Keep spare filters away from direct sunlight, humidity, and freezing temperatures.
Replace the air filter or PM2.5 filter every six months, or more frequently depending on sanitary conditions.
Using a dirty air filter may hinder device performance or cause damage.
Disinfection Guidelines
If the cleaning instructions are followed diligently, disinfection of the device or water chamber is usually unnecessary. However, if the device becomes contaminated or is used in clinical trials, disinfectants can be purchased to sanitize the device.
Disinfection of the Water Chamber:
Clean the water chamber first, following the instructions provided in the cleaning section.
For heat disinfection, soak the water chamber in water at 75°C ± 2°C for 30 minutes.
Mild disinfectants can also be used as per manufacturer instructions.
Disinfection of the SpO2 Probe:
Refer to the user manual for specific disinfection instructions for the SpO2 probe.
WARNINGS!
Thoroughly rinse disinfected components, especially those that come into direct contact with the patient (mask, headgear, tubing), to remove disinfectant residue. This prevents skin or respiratory irritation and allergic reactions.
Only recommended sterilization methods should be used for the device and its components.
To prevent cross-infection, a Breathing System Filter (BSF) certified to ISO 23328-1:2003 and ISO 23328-2:2002 standards can be used.
Always replace the BSF when using the device for different patients.
Monitor BSF resistance increase and blockage to ensure the device maintains normal pressure delivery.
CAUTIONS!
Disinfectants may damage materials and reduce their lifespan. Choose disinfectants carefully and follow the manufacturer’s guidelines.
After disinfection, inspect components for damage and replace any faulty parts immediately.
Traveling with the Device
Use the provided carrying case to transport the device and accessories. Avoid checking them in your luggage.
The device is compatible with power supplies ranging from 100 – 240 V and 50 / 60 Hz, making it suitable for worldwide use. You may need a power socket adapter.
Bring spare air filters and necessary emergency documentation from your physician.
At security stations, the device is labeled as a medical device, which may help streamline the screening process. It’s helpful to carry this manual for reference.
CAUTIONS!
Always empty the water chamber before traveling to prevent water from entering the device.
Verify the device’s altitude setting when traveling to avoid incorrect airflow pressures.
If atmospheric pressure is outside the specified range, it may affect the accuracy of the leak alarm.
Transferring the Device to Another Patient
Replace the mask, headgear, tubing, and air filter before transferring the device to another patient to prevent cross-infection.
Contraindications:
Clinicians should be aware that this device can deliver pressures up to 20 cmH2O, with a possible maximum of 40 cmH2O in certain fault conditions.
Studies indicate that the following pre-existing conditions may contraindicate CPAP therapy:
Bullous Lung Disease
Pathologically Low Blood Pressure
Bypassed Upper Airway
Pneumothorax
Pneumocephalus has been reported in patients using nasal Continuous Positive Airway Pressure (CPAP). Caution should be exercised for patients with the following conditions:
Cerebral Spinal Fluid (CSF) leaks
Abnormalities of the cribriform plate
History of head trauma
Pneumocephalus
The use of positive airway pressure therapy may be temporarily contraindicated if you show signs of:
Sinus infection
Middle ear infection
This device is not for use with patients whose upper airways are bypassed.
Always contact your healthcare professional if you have questions about your therapy.
Common errors
Error Types and Descriptions:
STOP:
Error data is saved in the non-volatile memory (NVRAM).
Device enters a “Safe State” where only limited functions are available (serial communication, turning off alarm, and powering down).
REBOOT:
Error information is logged in NVRAM, and the device automatically reboots.
Can be escalated to a STOP error if the “Verbose Mode” is enabled.
CONTINUE:
Error is logged in NVRAM, but the device continues functioning as normal.
Can also be escalated to a STOP error with the “Verbose Mode” setting.
LOG_ONLY:
Error is recorded in NVRAM, and the device operates without interruption.
Not escalated to a STOP error even in Verbose Mode.
General Errors:
E-1: Software issue causing a complete STOP.
E-3: Internal RAM error requiring reboot.
E-4: Null pointer error leads to reboot.
E-5: Data error requiring a reboot.
E-6: State machine issue leading to reboot.
E-7: Software-related error causing a reboot.
Watchdog and Timer Errors:
E-10: Watchdog RAM test failure—requires a reboot.
E-11: Watchdog test failure—triggers reboot.
E-12: Watchdog failure due to no card—requires reboot.
E-13: Watchdog failure related to SD card—reboot needed.
E-14: Low-resolution timer watchdog failure—requires reboot.
E-15: Cycle handler overrun—requires reboot.
E-16: Timeout during RASP restore—device continues operating.
E-17: Onems handler overrun—causes reboot.
E-19: Watchdog timeout—leads to reboot.
Motor / Blower Errors:
E-20: Low motor flux during spin-up—requires reboot.
E-21: High motor voltage (Vbus)—results in STOP.
E-22: Flux magnitude error in motor—causes reboot.
E-23: Motor overspeed—triggers reboot.
E-24: Reverse motor speed—leads to reboot.
E-25: Open thermistor in motor—device continues.
E-26: Shorted thermistor in motor—device continues.
E-27: Motor RL not converging—results in STOP.
E-28: Negative quadrature voltage—causes reboot.
E-29: Vbus gain set to zero—reboot required.
E-30: High motor flux during spin-up—triggers reboot.
NVRAM Low Level Errors:
E-40: NVRAM error—reboot needed.
E-41: Storage unit RAM failure—requires reboot.
E-42: Unable to obtain bus—results in reboot.
E-43: No callback occurred for NVRAM—requires a reboot.
E-44 to E-47: Various NVRAM buffer and callback issues—require reboot.
NVRAM Unit Related Errors:
E-50: Corrupt daily values—logged only.
E-51: Corrupt compliance log—device continues operating.
E-52: Compliance callback error—device continues.
E-53: Compliance log request overflow—requires reboot.
E-54: Therapy queue full—device continues.
E-56 to E-58: Various compliance log and session errors—reboot required.
General Hardware Errors:
E-60: Unsupported hardware—reboot required.
E-61: PLL unlocked—causes reboot.
E-62: Stuck ramp key—device continues.
E-63: Stuck knob key—device continues.
E-64: PWM overtime—causes reboot.
E-65 & E-66: Stuck encoder issues—device continues.
Pressure Sensor Errors:
E-70: Pressure sensor missing—results in STOP.
E-72: Unable to obtain bus for pressure sensor—reboot required.
E-73: Pressure sensor offset error—leads to STOP.
Flow Sensor Errors:
E-80: Unable to initialize flow sensor—causes reboot.
E-81: Flow sensor table error—device continues.
E-82: Flow sensor offset—device continues.
E-83: Unable to obtain bus for flow sensor—reboot required. Second failure escalates to STOP.
E-84: Flow sensor stopped—results in STOP.
E-85: Flow sensor occluded—device continues.
E-86 & E-87: Flow sensor issues—device continues.
OTP and RTC Errors:
E-90 & E-91: OTP not configured or misconfigured—results in STOP.
E-93: RTC value error—device continues.
E-94: RTC stopped—device continues.
Humidifier Errors:
E-100: No heat from humidifier—device continues.
E-101: Humidifier temperature too high—leads to STOP.
E-102 to E-105: Various thermistor and communication errors—device continues.
Stack and Exception Handler Errors:
E-110 to E-125: Various stack overflow, underflow, and exception handling errors—reboot required.