"Flex" bioexamination equipment - Taiwan Registration e8e20b6486b3432651f46c85a77122b2
Access comprehensive regulatory information for "Flex" bioexamination equipment in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e8e20b6486b3432651f46c85a77122b2 and manufactured by ENDO-FLEX GMBH. The authorized representative in Taiwan is IDS MEDICAL SYSTEMS (HONG KONG) COMPANY LIMITED, TAIWAN BRANCH (HONG KONG).
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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e8e20b6486b3432651f46c85a77122b2
Registration Details
Taiwan FDA Registration: e8e20b6486b3432651f46c85a77122b2
Device Details
"Flex" bioexamination equipment
TW: "็ฆ่ๅ
ๆฏ"็ๆชขๅจๆขฐ
Risk Class 2

