"Quirses" clarifies the compress
Taiwan·Risk Class 2·TearScience, Inc.;; Remington Medical, S.A.·Registered Sep 25, 2022 – Sep 25, 2027Active- Analysis ID
- cb32c061a397e98a3a70e684e8383f8e
- Customs Code
- DHA05603595301
- Manufacturer
- TearScience, Inc.;; Remington Medical, S.A.
- Manufacturer Country
- Dominican Republic;;United States
- Authorized Representative
- AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG)
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- M Ophthalmology
- Product Type (Level 2)
- M.5200 Eyelid Thermal Vibration System
- Import Information
- Input;; Contract manufacturing
- Registration Date
- Sep 25, 2022
- Expiry Date
- Sep 25, 2027
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Access comprehensive regulatory information for "Quirses" clarifies the compress in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cb32c061a397e98a3a70e684e8383f8e and manufactured by TearScience, Inc.;; Remington Medical, S.A.. The authorized representative in Taiwan is AMO ASIA LIMITED, TAIWAN BRANCH (HONG KONG).
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Remington Medical, Inc.;; TearScience, Inc., 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.