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"Gore" Predford pericardial replacement membrane - Taiwan Registration 42ae6b804a54e5d48c671f5a4287e344

Access comprehensive regulatory information for "Gore" Predford pericardial replacement membrane in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 42ae6b804a54e5d48c671f5a4287e344 and manufactured by 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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42ae6b804a54e5d48c671f5a4287e344
Registration Details
Taiwan FDA Registration: 42ae6b804a54e5d48c671f5a4287e344
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Device Details

"Gore" Predford pericardial replacement membrane
TW: "ๆˆˆ็ˆพ"ๆ™ฎ็‘žๅพ—็ฆๅฟƒๅŒ…่†œไปฃ็”จ่†œ
Risk Class 2

Registration Details

42ae6b804a54e5d48c671f5a4287e344

DHA00600772602

Company Information

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Dec 30, 1995

Jun 19, 2027