Medical Applications
There's no job more mission-critical than saving lives. Leading manufacturers of portable medical instruments look to Micro Power to keep their life-saving equipment running at peak performance. Whether the medical device is used for life-sustaining or life-saving operation, Micro Power can meet the stringent requirements demanded by medical OEMs.
Our battery and charger solutions are designed for optimal use by medical professionals in the most critical settings:
- Uniquely designed for the surgical suite
- Power solutions for hospital equipment
- Power solutions for emergency patient care
Micro Power has experience designing medical batteries and battery chargers for:
- Defibrillators (AED)
- Ultrasound devices
- Patient monitoring equipment
- Multi-parameter monitors
- Critical care monitors
- Infusion pumps
- Endoscopes
- Portable X-ray
- Intra-Aortic Balloon Pumps (IABP)
- Ventilators
- Surgical Instruments
Micro Power offers medical instrument manufacturers the highest quality standards:
- ISO 13485 and 9001: 2000 certified status
- Extensive experience in the design of medical batteries and battery chargers for the healthcare industry
- Maintaining one of the lowest Defects Per Million (DPM) rates in the entire portable power industry (less than 600 DPM)
- Risk mitigation of a potentially faulty manufacturing process can be achieved Process Failure Mode and Effect Analysis (PFMEA) of the manufacturing process
- Risk mitigation in the design process is achieved with Design Failure Mode and Effect Analysis (DFMEA)
- Identification and traceability is established by the manufacturing order and is maintained for each product order, recording, assembly, inspection, and test steps
- Traceability enables Micro Power to track and pinpoint the affected product (unfinished or finished product) within and outside our manufacturing facility
- Build in quality with next step inspection, final production tests & sign-offs on each production run
- Generateration and maintainance of Design History Files (DHF), and Device History Records (DHR). DHFs include any records which describe the design history of a device — design review notes, verification plan and results, validation plan and results, FMEA results. DHRs include documentation affiliated with production — test reports, test data, signed build documents, Certificate of Compliance (CoC), and quality assurance checklist
