Taiwan FDA registration 6ce64bbdfd89e31cf96d93ebc3db847a
“Long Term” LH TEST (Non-sterile)
TW: “龍騰” 排卵體外試劑組 (未滅菌)
Registration details
- Analysis ID
- 6ce64bbdfd89e31cf96d93ebc3db847a
- License Form
- Ministry of Health Medical Device Manufacturing No. 007187
Company information
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- Longteng Biotechnology Co., Ltd. new market factory
Product details
- 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
- Produced in Taiwan, China
Dates and status
- Registration Date
- Mar 23, 2018
- Expiry Date
- Mar 23, 2028
About this record
Access comprehensive regulatory information for “Long Term” LH 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 6ce64bbdfd89e31cf96d93ebc3db847a and manufactured by Longteng Biotechnology Co., Ltd. new market factory. The authorized representative in Taiwan is Longteng Biotechnology Co., Ltd. new market factory.
This page provides complete technical specifications, regulatory compliance details. 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.
Free DatabasePowered by Pure Global AI89,000+ Devices