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| Part Number: | MAX30001CWV+ |
|---|---|
| Manufacturer/Brand: | Analog Devices Inc./Maxim Integrated |
| Part of Description: | IC BIOPOTENTIAL AFE 30WLP |
| Datasheets: |
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| RoHs Status: | ROHS3 Compliant |
| Payment: | PayPal / Credit Card / T/T |
| Shipment Way: | DHL / Fedex / TNT / UPS / EMS |
| Share: |
Ship From: Hong Kong
| Quantity | Unit Price |
|---|---|
| 1+ | $2.8787 |
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| Product Attribute | Attribute Value |
|---|---|
| Type | Biopotential AFE |
| Supplier Device Package | 30-WLP (2.74x2.93) |
| Series | - |
| Package / Case | 30-WFBGA, WLBGA |
| Product Attribute | Attribute Value |
|---|---|
| Package | Strip |
| Mounting Type | Surface Mount |
| Base Product Number | MAX30001 |
| Applications | Heart Rate Monitoring |




The MAX30001CWV+ from Analog Devices Inc./Maxim Integrated represents a state-of-the-art single-channel analog front-end (AFE) designed for biopotential and bioimpedance signal acquisition. Packaged in a compact 30-bump WLP (2.74x2.93 mm), this solution targets high-performance clinical, fitness, and wearable medical electronics, supporting both electrocardiogram (ECG), R-to-R interval measurement, pacemaker edge detection, and bioimpedance (BioZ) sensing for respiration monitoring.
MAX30001CWV+ is engineered for ultra-low-power operation, providing extended battery life in portable systems. Its robust feature set enables compliance with IEC 60601-2-47:2012 ambulatory ECG standards, facilitating rapid development and reliable performance in regulated medical devices. The module’s versatility means it is equally applicable to event monitors, wireless patient patches, heart rate chest bands, bio-authentication devices, and impedance-based health monitors.
MAX30001CWV+ is characterized by its clinical-grade analog design and precision data conversion, delivering performance metrics such as 15.9 ENOB (Effective Number of Bits) at 3.1 µVpp noise for ECG and 17 ENOB at 1.1 µVpp noise for BioZ. A differential input structure provides >100 dB common-mode rejection ratio (CMRR), while input impedance exceeding 1 GΩ ensures minimal signal attenuation in challenging electrode environments.
The device accommodates high DC electrode offsets (±650mV at 1.8V) and boasts an AC dynamic range of 65mVpp for ECG and 90mVpp for BioZ, optimizing saturation resistance during motion or electrode impacts. Power consumption is impressively low, with 85 µW during ECG monitoring and 158 µW for BioZ functions, facilitating deep sleep operation of the host microcontroller until lead-on detection or valid signal interrupts arise.
MAX30001CWV+ integrates numerous hardware features to boost system robustness, such as ESD protection (±8kV contact, ±15kV air gap), EMI filtering, input biasing options, built-in calibration voltages, soft power-up sequencing, and high-speed SPI communication. The internal FIFO architecture (32 words for ECG, 8 words for BioZ) allows uninterrupted data capture and system controller power-downs up to 256ms, all backed up by intuitive interrupt-driven design.
At a system level, MAX30001CWV+ comprises dedicated analog channels for biopotential and bioimpedance measurement, each built around a sophisticated input multiplexer, programmable instrumentation amplifier, anti-alias filters, programmable gain amplifiers, and sigma-delta ADCs (18-bit for ECG, 20-bit for BioZ). The input MUXes are equipped with DC and AC leads-off/lead-on detection, ESD/EMI protection, isolation switches, internal bias resistors, and programmable calibration sources for self-test and system checking.
All signal processing and data management are performed within the device, offering configurability for gain, filter corner frequencies, and interrupt thresholds through the SPI register interface. The overall architecture is optimized for minimal signal distortion, rapid recovery from overdrive events (e.g., defibrillation), and seamless multiplexing between different measurement modes.
For ECG acquisition, the MAX30001CWV+ delivers industry-leading noiseless signal amplification through a fixed-gain (20V/V) differential amplifier, followed by a 2-pole anti-aliasing filter (600 Hz, -3dB) and programmable gain amplifier (1, 2, 4, or 8 V/V steps). The analog front end employs chopping techniques to suppress offset and low-frequency (1/f) noise, delivering accurate waveforms suitable for both heart rate (preferably 5 Hz high-pass cutoff) and ambulatory patient monitoring (recommended 0.05 Hz cutoff for maximal waveform fidelity).
Leads-off detection (using programmable DC currents with adjustable voltage windows) and ultra-low-power leads-on interrupts allow for robust handling of electrode contact issues in dynamic environments. Fast recovery mode, automatically or manually triggered, ensures that the amplifier rapidly resumes normal operation after overdrive events—critical in clinical scenarios with defibrillation shocks or pacing signals.
ECG data is output in 18-bit left-justified format, easily convertible to absolute voltage values for digital post-processing. Hardware-based R-to-R interval detection, utilizing a Pan-Tompkins algorithm adaptation, generates heart rate interrupts with timing resolution down to 8ms, minimizing firmware processing load and allowing power-efficient event monitoring.
The BioZ channel features a similar analog architecture to the ECG channel but adds a mixer, programmable current generator, and robust output calibration mechanisms. Bioimpedance measurements enable respiration monitoring and hydration analysis by injecting modulated AC currents (8–96 µA peak, 125 Hz–131 kHz frequency range) through dedicated electrodes and sensing the differential response.
Compliance monitoring, DC/AC leads-off detection (with multi-threshold comparators), and programmable resistive test loads support reliable measurement and diagnostic self-tests. The input MUX incorporates AC lead-off detection and programmable load modulation for end-to-end channel verification. The device supports both two-electrode and four-electrode configurations, with current amplitude and phase tuning for accurate measurements over variable body impedances. Data is presented in 20-bit format, with built-in conversion equations for direct post-processing into ohms.
MAX30001CWV+ leverages a high-speed SPI interface for digital configuration and real-time data transfer, compatible with standard SPI, QSPI, Microwire, and DSP protocols. The 32-cycle instruction frame comprises command/address plus 24-bit data, supporting both normal and burst mode reads to efficiently access FIFO-stored measurements. Interrupt outputs (INTB, INT2B), with programmable masking and open-drain or CMOS output options, allow precise event-driven communication with microcontrollers.
Register architecture provides fine-grained control of all AFE operations: acquisition parameters, filter settings, gain adjustments, calibration source routing, and synchronization commands for FIFO and DSP filter resets. Example engineering scenarios include interrupt-driven ECG and BioZ readouts, FIFO-based power management, and burst-mode data acquisition optimization.
MAX30001CWV+ is ideally suited for single-lead event monitors, in-patient/out-patient wireless patches, fitness heart rate wearables, bio-authentication systems, and respiration monitors. This versatility is rooted in its robust analog design, ultra-low power modes, and hardware-accelerated physiological event detection.
Real-world engineering best practices include external EMI suppression for demanding environments, judicious selection of high-pass filter corner frequencies based on monitoring requirements, and leveraging internal or external body biasing for improved electrode signal integrity. The device directly supports IEC 60601-2-47 compliance for ambulatory ECG systems via built-in safety and performance features, supporting streamlined medical certification.
The MAX30001CWV+ is fabricated in CMOS and supplied in a 30-bump wafer-level package. The recommended operating temperature range is 0°C to +70°C, with ample safety margins in storage and soldering. Absolute maximum voltage, current, and thermal ratings are specified to ensure reliability across lifespan and integrating environments.
Package-level ESD and thermal resistance are consistent with JEDEC JESD51-7 specifications. The device footprint, land pattern, and external filtering recommendations are provided to facilitate PCB design for compact wearables and medical modules.
For projects requiring similar functionality, potential alternatives to the MAX30001CWV+ from Analog Devices Inc./Maxim Integrated include earlier MAX3000x series biopotential AFEs or comparable AFE solutions from other global analog IC vendors specializing in medical-grade ECG and BioZ channels. Key considerations in selecting replacements include matching input noise performance, support for hardware ECG and bioimpedance channels, built-in ESD/EMI protection, interrupt and power management schemes, and adherence to medical device standards such as IEC 60601-2-47.
When evaluating equivalent models, engineers should compare analog input architecture, data converter ENOB ratings, ultra-low-power functions, FIFO capacity, and clinical certification status to ensure seamless substitution or migration.
: Engineering Value of MAX30001CWV+ Biopotential and Bioimpedance AFE
In summary, the MAX30001CWV+ from Analog Devices Inc./Maxim Integrated sets a benchmark for single-channel biopotential and bioimpedance analog front ends deployed in modern clinical, wearable, and fitness monitoring electronics. Its ultra-low-power operation, high fidelity signal pathways, hardware-based physiological event detection, and robust digital interfacing combine to minimize system complexity while maximizing measurement accuracy and reliability.
Engineers and procurement professionals evaluating device selection benefit from its integrated safety, compliance, and self-test features, as well as streamlined system power management support. When building next-generation ECG, heart rate, and respiration monitoring solutions, the MAX30001CWV+ offers a proven foundation consistent with the rigorous demands of ambulatory, wearable, and medical device engineering.
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