"ASTF" cold compress (unsterilized) - Taiwan Registration 9ef102e498b2981aa2a1fac991c0af13
Access comprehensive regulatory information for "ASTF" cold compress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9ef102e498b2981aa2a1fac991c0af13 and manufactured by Venice Pharmaceutical Factory Ltd;; Honglin Pharmaceutical Co., Ltd. The authorized representative in Taiwan is HON LIN PHARMACEUTICAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including VENICE LABORATORIES CO., LTD., and 1 recent registrations in the same category. 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.
Device Details
Product Details
Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
o Physical Medical Sciences
O.5700 ้ซ็็จๅท็ฑๆท่ฃ็ฝฎ
Domestic;; Contract manufacturing
Dates and Status
Oct 01, 2021
Oct 31, 2023
Nov 02, 2023
Cancellation Information
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