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Fore collagen biofilm - Taiwan Registration 9a51f0e2dfc4d5373c79dddfd16bf6fc

Access comprehensive regulatory information for Fore collagen biofilm in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 9a51f0e2dfc4d5373c79dddfd16bf6fc and manufactured by Asia Fruit Medical Co., Ltd.;; Taibo Technology Co., Ltd. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

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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9a51f0e2dfc4d5373c79dddfd16bf6fc
Registration Details
Taiwan FDA Registration: 9a51f0e2dfc4d5373c79dddfd16bf6fc
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Device Details

Fore collagen biofilm
TW: ็ฆ็ˆพ่† ๅŽŸ่›‹็™ฝ็”Ÿ็‰ฉ่†œ
Risk Class 2

Registration Details

9a51f0e2dfc4d5373c79dddfd16bf6fc

Company Information

Product Details

Details are as detailed as approved Chinese instructions

F Dentistry

F.3930 Alveolar repair materials

Contract manufacturing;; Domestic

Dates and Status

Jul 19, 2024

Aug 20, 2028