“Artron” One Step Rapid Diagnostic Test - Ovulation LH Strip Test (Non-Sterile)
- Analysis ID
- 7e8ba4d1eea7f81a90e954679def6eaa
- License Form
- Ministry of Health Medical Device Import No. 019517
- Customs Code
- DHA09401951709
- Manufacturer
- ARTRON LABORATORIES INC.
- Manufacturer Country
- Canada
- Authorized Representative
- WEIYOU TECH INC.
- Intended Use
- Limited to the first level recognition range of the "Luteinizing hormone test system (A.1485)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1485 Progesterone Test System
- Import Information
- Imported from abroad
- Registration Date
- Aug 21, 2018
- Expiry Date
- Aug 21, 2023
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Access comprehensive regulatory information for “Artron” One Step Rapid Diagnostic Test - Ovulation LH Strip Test (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 7e8ba4d1eea7f81a90e954679def6eaa and manufactured by ARTRON LABORATORIES INC.. The authorized representative in Taiwan is WEIYOU TECH INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ARTRON LABORATORIES 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.