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Seisa +
ProtoQuick & Peridot
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Call or Click to Email:
(+1-800-495-3323)
Call or Click to Email: (+1-800-495-3323)
Seisa’s commitment to precision, innovation, and excellence means we are always seeking motivated individuals to grow our contribution to improving lives through the medical device industry.
Seisa has 30 years’ experience in compliance with FDA and international regulations and audits, delivering Class III devices for 15 years. Our global facilities are ISO-13485 certified. Seisa’s multiple 510K product registration approvals are a testament to the rigor of our development capabilities.
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