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"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
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Device Details

"Flex" balloon expansion catheter
TW: โ€œ็ฆ่Šๅ…‹ๆ–ฏโ€ๆฐฃ็ƒๆ“ดๅผตๅฐŽ็ฎก
Risk Class 2

Registration Details

4284ff983c0812e38a2af673397fe139

DHA00602371400

Company Information

Product Details

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

H Gastroenterology and urology

H.1500 Internal Scope and its accessories

import

Dates and Status

Jul 18, 2012

Jul 18, 2022