Taiwan FDA registration ed502971199a7ebd0c9de4b8f2bbf3f2
Flexicon Ovulation Test (Unsterilized)
TW: 易利康 排卵測試 (未滅菌)
Registration details
- Analysis ID
- ed502971199a7ebd0c9de4b8f2bbf3f2
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- NEW YING CHENG CO., LTD.
Product details
- Intended Use
- Limited to the classification and grading management measures of medical equipment "Luteinizing hormone test system (A.1485)" first level identification range.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- 委託製造;; 國產;; QMS/QSD
Dates and status
- Registration Date
- Jun 24, 2016
- Expiry Date
- Jun 24, 2026
About this record
Access comprehensive regulatory information for Flexicon Ovulation Test (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ed502971199a7ebd0c9de4b8f2bbf3f2 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is NEW YING CHENG CO., LTD..
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.
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