“Helena” CSF Protein reagent kit (Non-sterile)
Taiwan·Risk Class 1·MD·HELENA LABORATORIES INC.·Registered May 14, 2014 – May 14, 2019Cancelled- Analysis ID
- e8ae41b20b842cf2b5108c6c7af3354c
- License Form
- Ministry of Health Medical Device Import No. 014140
- Customs Code
- DHA09401414002
- Manufacturer
- HELENA LABORATORIES INC.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1630 Protein (Chemical Separation) Test System
- Import Information
- Imported from abroad
- Registration Date
- May 14, 2014
- Expiry Date
- May 14, 2019
- Cancellation Date
- Jun 16, 2022
- Status
- Logged out
- Reason
- 許可證已逾有效期未申請展延
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Access comprehensive regulatory information for “Helena” CSF Protein reagent kit (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 e8ae41b20b842cf2b5108c6c7af3354c and manufactured by HELENA LABORATORIES INC.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HELENA LABORATORIES CORP., 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.