Taiwan FDA registration 1b22b1aa06722b82cbd669572e700b43
Mingjie rapid pregnancy test reagent
TW: 明傑快速驗孕試劑
Taiwan·Risk Class 2·TONYAR BIOTECH. INC.·Registered Oct 16, 2012 – Sep 28, 2015CancelledRegistration details
- Analysis ID
- 1b22b1aa06722b82cbd669572e700b43
Company information
- Manufacturer
- TONYAR BIOTECH. INC.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- MIN JIER FIRM
Product details
- Intended Use
- 利用定性法進行血清或尿液中是否含有人類絨毛膜刺激生殖激素(HCG, human chorionic gonadotropin)之測試.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1155 Human chorionic gonadotropin testing system
- Import Information
- Contract manufacturing;; Domestic
Dates and status
- Registration Date
- Oct 16, 2012
- Expiry Date
- Sep 28, 2015
- Cancellation Date
- Jan 30, 2018
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for Mingjie rapid pregnancy test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 1b22b1aa06722b82cbd669572e700b43 and manufactured by TONYAR BIOTECH. INC.. The authorized representative in Taiwan is MIN JIER FIRM.
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