"ASTF" cold compress (unsterilized)
Taiwan·Risk Class 1·Venice Pharmaceutical Factory Ltd;; Honglin Pharmaceutical Co., Ltd·Registered Oct 01, 2021 – Oct 31, 2023Cancelled- Analysis ID
- 9ef102e498b2981aa2a1fac991c0af13
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- HON LIN PHARMACEUTICAL CO., LTD.
- Intended Use
- Limited to the classification and grading management of medical equipment, the first level identification range of "Medical Hot and Cold Compress Device (O.5700)".
- Product Type (Level 1)
- o Physical Medical Sciences
- Product Type (Level 2)
- O.5700 醫療用冷熱敷裝置
- Import Information
- Domestic;; Contract manufacturing
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
- Cancellation Date
- Nov 02, 2023
- Status
- Logged out
- Reason
- 未展延而逾期者
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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.