IEC/UL 60601 Compliant 24V 7A Desktop Medical Power Adapter & Switching Power Supply 2×Mopp Isolation UL CE Ukca Rcm

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Product Description

Basic Specifications
Model NO.
APM150DB
Certification
TUV, RoHS, ISO9001, CCC, CE, Ukca, UL, Rcm, PSE, Kc
Color
Black or White
Output Voltage
12V~48V
Output Current
3.0A~14.0A
Rate Power
168W Max
Input
100~240VAC, 50/60Hz
Safety Spec
IEC/EN/UL 60601-1
Product Overview

IEC/UL 60601 Compliant 24V 7A Desktop Medical Power Adapter & Switching Power Supply | 2×MOPP Isolation | UL CE UKCA RCM

This 168W (24V 7A) desktop medical power adapter is engineered to the highest safety standards for patient-connected equipment, fully compliant with IEC 60601-1:2012 (4th Edition) and its regional equivalents. It features 2×MOPP (Means of Patient Protection) isolation—providing two independent layers of protection between the mains input and the patient-accessible output—making it suitable for BF-type applied parts in direct or indirect contact with patients.

Key Features & Benefits
  • 2×MOPP Isolation - Provides dual patient protection per IEC 60601-1 Clause 8.5
  • BF-Type Applied Part Ready - Designed for equipment with conductive contact with a patient's body
  • Multi-Market Certified - Valid UL, CE, UKCA, and RCM certifications under 4th Ed standards
  • Ultra-Low Leakage Current - Patient leakage: <10 µA (normal), <50 µA (single-fault)
  • Reinforced Insulation - Primary-to-secondary isolation tested at 4000 VAC
  • Low Ripple (<150 mV p-p) - Ensures signal integrity in sensitive analog medical equipment
Model Comparison & Technical Parameters
Model Max Power Voltage Max Load Regulation Ripple & Noise
APM150DA150W24V6.25A±5%100mV
APM150DB168W24V7.0A±5%100mV
APM150DC150W36V4.17A±5%100mV
APM150DD168W36V4.67A±5%100mV
APM150DE150W48V3.13A±5%100mV
APM150DF168W48V3.5A±5%100mV
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Manufacturing Excellence

Automated Production

Manufactured by fully automated lines operating 24/7, ensuring ultra-high efficiency and fast delivery cycles for large orders.

Consistent Quality

Robotic precision eliminates human error, providing stable voltage and current output with ultra-low defect rates.

Cost Efficiency

Automation reduces labor costs by 80%, allowing us to offer premium medical-grade power solutions at competitive prices.

Production Line
Ideal Applications
  • Home-use patient monitors and telehealth devices
  • Infusion pumps and respiratory therapy equipment (CPAP, ventilators)
  • Portable ultrasound and diagnostic imaging systems
  • Dental chairs and surgical workstations
After-sales & Warranty

24-Month Warranty: Coverage for materials and workmanship under normal use.

30-Day Return/Exchange: Available for unused products in original packaging.

Technical Support: Free consultation for installation and troubleshooting.

Quality Control
Frequently Asked Questions
What does 2×MOPP mean for medical safety?
2×MOPP (Means of Patient Protection) indicates the power supply has two independent insulation barriers. This ensures that even if one protection layer fails, the patient remains safe from electrical hazards, meeting the strict requirements of IEC 60601-1.
Is this power supply suitable for BF-type medical devices?
Yes, it is specifically designed for BF (Body Floating) type applied parts, which are medical devices that may have conductive contact with the patient, such as ventilators or monitors.
Does this adapter support global voltage standards?
Yes, it features a universal input range of 100-240V AC at 50/60Hz, making it compatible with power grids worldwide.
What is the leakage current of this medical adapter?
The adapter features ultra-low patient leakage current: less than 10 µA under normal conditions and less than 50 µA during single-fault conditions, ensuring maximum patient safety.
What certifications are provided for international markets?
The product is fully certified with UL, CE, UKCA, RCM, TUV, RoHS, and PSE, ensuring compliance for North America, Europe, UK, Australia, and Japan.
Can this be used for cardiac floating (CF) applications?
This adapter is designed for BF-type applications. It is not intended for CF-type (cardiac floating) applications unless further validated by the end-device manufacturer as part of a complete risk management process.

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