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Medical
The Federal Food and Drug Administration has long mandated the safety and effectiveness of
devices used in the medical industry. As an EMS company serving the medical market segment, many
Suntron customers require strict quality requirements that follow FDA-Good Manufacturing Practice
(cGMP) standards defined by the FDA 21 CFR Part 820 QSR. This QSR, commonly known as GMP, forces
manufacturers to implement a quality system for design, manufacturing, packaging, labeling,
storage and delivery for medical devices sold within the United States.
In addition to our ISO 13485 quality standard, our GMP registration allows Suntron to ensure
the highest quality level throughout our manufacturing processes. Our GMP status further enhances
our ability to support our Medical OEM customers by shipping products manufactured at Suntron
directly to the OEM customer’s required location.
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Medical Product Experience
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- Oral Cancer Monitoring & Diagnostic
- Neuroprosthetic Electrical Stimulation
- Flow Cytometry for Cell Analysis
- Positron Emission Tomography (PET)
- Ultrasound
- Endoscopy
- IV Drip Controller
- Electrosurgical Device
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- Fluorescent Angiographic System
- Collection System for Blood Cells
- Cryolipolysis
- Patient Monitoring and Connectivity
- High End Analytical Instrumentation
- Asset Tracking for Hospitals
- Corneal Topography
- Audiology Test System
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In an environment where quality and reliability are crucial aspects of manufacturing, Suntron
prides itself on a proven track record of customer satisfaction and on-time delivery.
If you would like additional information, please contact Suntron at info@suntroncorp.com.
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