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XM-101
Joytech / OEM
The XM-101 Bluetooth Fingertip Pulse Oximeter is a compact, lightweight, and user-friendly device designed to deliver accurate real-time monitoring of blood oxygen saturation (SpO₂), pulse rate (PR), perfusion index (PI), and waveform.
With low power consumption and a highly portable design, it is ideal for both home use and on-the-go health management.
Featuring five display modes with adjustable brightness levels (1–5), the device ensures clear readings in various lighting conditions.
It also provides a pulse bar graph and waveform display, helping users better understand their cardiovascular status.
The visual low-voltage warning alerts users when battery power is insufficient, while the auto power-off function activates within 10 seconds of detecting "Finger out", conserving energy.
The XM-101 also includes a beep and reminder function: when enabled, the display will flash and the buzzer will sound as an additional alert, enhancing user awareness.
With Bluetooth connectivity, results can be conveniently transferred and tracked on compatible smart devices, offering a more connected health monitoring experience.
Compact, reliable, and easy to operate, the XM-101 is a safe and practical solution for families who want to monitor oxygen saturation and heart rate comfortably at home.
Beep and tips
Automatic power-off
Light weight and easy to carry
Adjustable brightness, 5 display modes
Intelligent power saving design, 2 "AAA" batteries
Dual color display, 360° rotatable view
Model | XM-101/XM-111 |
Type | Fingertip pulse oximeter |
Measurement Method | Transmission-type |
Display Type | Dual-color display |
SpO2 Display Range | 0%-100% |
SpO2 Measurement Range | 70%-100% |
Pulse Rate Display Range | 0-240bpm |
Pulse Rate Measurement Range | 30-240bpm |
Running Conditions | 5-40℃ |
Display Size | 0.96 inch |
Humidity | 15%-93%RH |
Pressure | 700hPa-1060hPa |
SpO2 | Yes |
Pulse Rate | Yes |
Adjustable Brightness | Yes |
Display Modes | 5 |
Automatic Power-off | Yes |
Beeps | Yes |
Low Oxygen Content | Yes |
Bluetooth | Optional |
Power Source | 2“AAA”batteries |
Finger off Remind | Yes |
Power Dissipation | < 60mA |
The Data UPDATE Period | < 12S |
RED | Approx. 660nm Approx. 3.2mW |
IR | Approx. 905nm Approx. 2.4mW |
Unit Dimension | 60.2x35x35.5mm |
Unit Weight | Approx. 54g |
Packing | 1 pc / Gift box; 60 pcs / Carton |
Carton Dimensions | 36x22.5x35cm |
Carton Weight(G.W.) | 6.7kg |
• 24 years of OEM & ODM expertise.
• 3 manufacturing centers with 260,000㎡ automated facilities and 2000㎡ automated warehouses.
• 30+ production lines & 100+ patented innovations.
• ISO 13485, MDSAP, BSCI certified quality systems.
• Full customization for global brands, including Fortune 500 partners.

• WHX Dubai (formerly Arab Health), Dubai
• WHX Miami (formerly FIME), Miami, USA
• Hong Kong Electronics Fair, Hong Kong
• ABC Kids Expo, USA
• KIMES, Seoul, Korea
• MEDITEX Bangladesh, Dhaka
• Hospitalar, São Paulo, Brazil
• Canton Fair, China
• MEDICA, Düsseldorf, Germany
We are committed to meeting partners worldwide at leading international medical and consumer health exhibitions.

Q: How does the Bluetooth function enhance monitoring for families?
A: It allows multiple users to sync their readings to a smartphone app. This enables the whole family to track individual SpO₂ and pulse rate trends conveniently in one place.
Q: How do the display modes help in different situations?
A: The 5 display modes and adjustable brightness let you customize the screen view for clarity, whether in a dark room at night or in bright daylight, ensuring the readings are always easy to see.
Q: What makes this model a practical choice for home health management?
A: Its combination of medical-grade accuracy, simple one-button operation, and the ability to log data via Bluetooth makes it a reliable and user-friendly tool for keeping an eye on the wellness of all family members.
For customized solutions or partnership inquiries, please contact us at marketing@sejoygroup.com to discuss your specific needs.
1. Before use, carefully read the manual.
2. Do not use the pulse oximeter:
-If you are allergic to rubber products.
-If the device or finger is damp.
-During MRI or CT scan.
-While taking a blood pressure measurement on the arm.
-Nail polish, dirty, coating fingers and false nails applied fingers.
-Fingers with anatomical changes, edemas, scars or burns.
-Too big finger: the width of finger is over than 20mm and the thickness is over than 15mm.
-Too small finger: the width of finger is less than 10mm and the thickness is less than 5mm.
-Minors under 18 years old.
-The environmental light changes strongly.
-Near flammable or explosive gas mixtures.
3. Extended use may cause pain for people with circulatory disorders. Do not use the pulse oximeter for longer than two hours on one finger.
4. Measurements are for your information only - they are no substitute for a medical examination. If an unexpected reading occurs, the operator can take several more measurements and consult a doctor.
5. Check the pulse oximeter regularly before use to ensure that there is no visible damage and the batteries are still sufficiently charged. In case of doubt, do not use the device and contact customer services or authorized retailer.
6. Do not use any additional parts that are not recommended by the manufacturer.
7. Any circumstances do not open or repair the device by yourself. Failure to comply will result in voiding of the warranty. For repairs, please contact customer services or authorized retailer.
8. Do not look directly inside the housing during the measurement. The red light and the invisible infrared light in the pulse oximeter are harmful to your eyes.
9. This device is not intended for use by people (including children) with restricted physical, sensory or mental skills or a lack of experience or a lack of knowledge, unless they are supervised by a person who has responsibility for their safety or they receive instructions from this person on how to use the device. Children should be supervised around the device to ensure they do not play with it.
10. If the unit has been stored at temperatures below 0℃, leave it in a warm place for about two hours before using it.
11. If the unit has been stored at temperatures above 40 , leave it in a cool place for about two hours before using it.
12. The displays for the pulse bar does not allow the strength of the pulse or circulation to be evaluated at the measurement site. Rather, they are exclusively used to display the current visual signal variation at the measurement site and do not enable diagnostics for the pulse.
13. Operation of the fingertip pulse oximeter may be affected by the use of an electrosurgical unit (ESU).
14. Follow local ordinances and recycling instructions regarding disposal or recycling or the device and device components, including batteries.
15. This equipment complies with IEC 60601-1-2 for electromagnetic compatibility for medical electrical equipment and systems. In healthcare center or other environment, their radio transmission equipment and electromagnetic interference may affect the performance of the oximeter.
16. This equipment is not intended for use during patient transport outside the healthcare facility.
17. When the signal is not stable, the reading may inaccurate. Please do not reference.
18. Portable and mobile RF communications equipment can affect medical electrical equipment.
19. WARNING: Use of this equipment adjacent to or stacked with other equipment should be avoided because it could result in improper operation. If such use is necessary, this equipment and the other equipment should be observed to verify that they are operating normally.
20. WARNING: PORTABLE RF communications equipment (includeing peripherals such as antenna cables and external antennas) should be used no closer than 30cm (12 inches) to any part of Fingertip Pulse Oximeter, including cables specified by the MANUFACTURER. Otherwise, degradation of the performance of this equipment could result.
21. Any serious incident that has occurred in relation to the device should be reported to the manufacture and the competent authority of the Member State in which the user and/or patient is established.