Taiwan FDA registration fa8cf5bf50de2548fff873fe8c58095c

"WONDFO" LH Ovulation Test (Non-Sterile)

TW: "雅創" 排卵檢測試劑 (未滅菌)

Taiwan·Risk Class 1·MD·GUANGZHOU WONDFO BIOTECH CO., LTD.·Registered Nov 27, 2018 – Nov 27, 2023Expired

Registration details

Analysis ID: fa8cf5bf50de2548fff873fe8c58095c
License Form: Ministry of Health Medical Device Land Transport No. 003615
Customs Code: DHA09600361502

Company information

Manufacturer: GUANGZHOU WONDFO BIOTECH CO., LTD.
Manufacturer Country: China
Authorized Representative: GORED ENTERPRISE CO., LTD.

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: Imported from abroad; Made in China

Dates and status

Registration Date: Nov 27, 2018
Expiry Date: Nov 27, 2023

About this record

Access comprehensive regulatory information for "WONDFO" LH Ovulation 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 fa8cf5bf50de2548fff873fe8c58095c and manufactured by GUANGZHOU WONDFO BIOTECH CO., LTD.. The authorized representative in Taiwan is GORED ENTERPRISE CO., LTD..

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