"Flex" esophageal dilator - Taiwan Registration 7be9fb85bf73f2a5119b9dffef833d35
Access comprehensive regulatory information for "Flex" esophageal dilator in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7be9fb85bf73f2a5119b9dffef833d35 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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7be9fb85bf73f2a5119b9dffef833d35
Registration Details
Taiwan FDA Registration: 7be9fb85bf73f2a5119b9dffef833d35
Device Details
"Flex" esophageal dilator
TW: "็ฆ่ๅ
ๆฏ"้ฃ้ๆดๅผตๅจ
Risk Class 2

