"Helena" QuickGel Lactate Dehydrogenase Reagent kit (Non-sterile)
- Analysis ID
- efa589240037898364b9a2ac050ef656
- License Form
- Ministry of Health Medical Device Import No. 018623
- Customs Code
- DHA09401862303
- Manufacturer
- HELENA LABORATORIES CORP.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
- Intended Use
- Limited to the first level recognition range of lactate dehydrogenase test system (A.1440) of the management method for medical devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1440 Lactate dehydrogenase test system
- Import Information
- Imported from abroad
- Registration Date
- Dec 19, 2017
- Expiry Date
- Dec 19, 2022
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Access comprehensive regulatory information for "Helena" QuickGel Lactate Dehydrogenase 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 efa589240037898364b9a2ac050ef656 and manufactured by HELENA LABORATORIES CORP.. 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, 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.