Taiwan FDA registration 5f3d8487547f2501ec74ce5892bfb180

Hanquan Ovulation Test Rapid Test Reagent (Unsterilized)

TW: 翰銓驗排卵快速檢驗試劑 (未滅菌)

Taiwan·Risk Class 1·TONYAR BIOTECH. INC.·Registered Jul 11, 2007 – Jul 11, 2027Active

Registration details

Analysis ID: 5f3d8487547f2501ec74ce5892bfb180
Customs Code: DHY04300192507

Company information

Manufacturer: TONYAR BIOTECH. INC.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HAN CHUAN MEDICAL MATERIAL BIO-TEC 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: Contract manufacturing;; Domestic

Dates and status

Registration Date: Jul 11, 2007
Expiry Date: Jul 11, 2027

About this record

Access comprehensive regulatory information for Hanquan Ovulation Test Rapid Test Reagent (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 5f3d8487547f2501ec74ce5892bfb180 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is HAN CHUAN MEDICAL MATERIAL BIO-TEC 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.