“Boditech” AFIAS-6 Analyzer (Non-Sterile)
Taiwan·Risk Class 1·MD·Boditech Med Inc.·Registered Oct 01, 2021 – Oct 31, 2026Active- Analysis ID
- 585308d9078df29f1a2f00e39384f4b1
- License Form
- Ministry of Health Medical Device Import Registration No. 022470
- Customs Code
- DHA08402247000
- Manufacturer
- Boditech Med Inc.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- PROGRESSIVE GROUP INC.
- Intended Use
- Limited to the first level identification range of the "Individual Photometric Chemical Analyzer for Clinical Use (A.2160)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A2160 Individual photometric chemistry analyzer for clinical use
- Import Information
- Imported from abroad
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2026
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Access comprehensive regulatory information for “Boditech” AFIAS-6 Analyzer (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 585308d9078df29f1a2f00e39384f4b1 and manufactured by Boditech Med Inc.. The authorized representative in Taiwan is PROGRESSIVE GROUP INC..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Boditech Med 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.