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"Sanyo Electronics" plasmapheresis filter - Taiwan Registration 295cbb0c68f695e40826517b092fde5d

Access comprehensive regulatory information for "Sanyo Electronics" plasmapheresis filter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 295cbb0c68f695e40826517b092fde5d and manufactured by SANYO ELECTRONIC INDUSTRIES CO., LTD.. The authorized representative in Taiwan is K2 INTERNATIONAL MEDICAL INC..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.

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295cbb0c68f695e40826517b092fde5d
Registration Details
Taiwan FDA Registration: 295cbb0c68f695e40826517b092fde5d
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Device Details

"Sanyo Electronics" plasmapheresis filter
TW: โ€œๅฑฑ้™ฝ้›ปๅญโ€่ก€ๆผฟ็ฝฎๆ›้ŽๆฟพๆฉŸ
Risk Class 2

Registration Details

295cbb0c68f695e40826517b092fde5d

DHA00602216300

Company Information

Product Details

For details, it is Chinese approved copy of the imitation order

H Gastroenterology and urology

H.5665 ้€ๆž็”จๆฐดไน‹ๆทจๅŒ–็ณป็ตฑ

import

Dates and Status

Feb 17, 2011

Feb 17, 2026