"Flex" balloon expansion catheter - Taiwan Registration 4284ff983c0812e38a2af673397fe139
Access comprehensive regulatory information for "Flex" balloon expansion catheter in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 4284ff983c0812e38a2af673397fe139 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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4284ff983c0812e38a2af673397fe139
Registration Details
Taiwan FDA Registration: 4284ff983c0812e38a2af673397fe139
Device Details
"Flex" balloon expansion catheter
TW: โ็ฆ่ๅ
ๆฏโๆฐฃ็ๆดๅผตๅฐ็ฎก
Risk Class 2

