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"Gore" sealing valve Frix guide sheath - Taiwan Registration d137054eaacfa99f9c14b0aebf238572

Access comprehensive regulatory information for "Gore" sealing valve Frix guide sheath in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d137054eaacfa99f9c14b0aebf238572 and manufactured by Creganna Medical;; W.L. Gore & Associates, Inc.. The authorized representative in Taiwan is W.L. GORE & ASSOCIATES (HONG KONG) LTD. TAIWAN BRANCH (H.K.).

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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d137054eaacfa99f9c14b0aebf238572
Registration Details
Taiwan FDA Registration: d137054eaacfa99f9c14b0aebf238572
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Device Details

"Gore" sealing valve Frix guide sheath
TW: โ€œๆˆˆ็ˆพโ€ๅฏ†ๅฐ้–ฅ็ฆ็‘žๅ…‹ๆ–ฏๅฐŽ้ž˜
Risk Class 2

Registration Details

d137054eaacfa99f9c14b0aebf238572

DHA05603261202

Company Information

Product Details

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

E Cardiovascular Medicine Science

E.1340 Catheter Introducers

Input;; Contract manufacturing

Dates and Status

May 24, 2019

May 24, 2029