Taiwan FDA registration 0cfff06b18188e926e1733d81d3e84c5
"MP" Progesterone Test (Non-Sterile)
TW: "馬丁彼得" 黃體脂酮檢驗試劑 (未滅菌)
Taiwan·Risk Class 1·MD·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Jul 21, 2014 – Jul 21, 2024ExpiredRegistration details
- Analysis ID
- 0cfff06b18188e926e1733d81d3e84c5
- License Form
- Ministry of Health Medical Device Import No. 014348
- Customs Code
- DHA09401434800
Company information
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Limited to the first level identification range of the "Progesterone Test System (A.1620)" of the Measures for the Administration of Medical Devices.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A1620 Progesterone Test System
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Jul 21, 2014
- Expiry Date
- Jul 21, 2024
About this record
Access comprehensive regulatory information for "MP" Progesterone 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 0cfff06b18188e926e1733d81d3e84c5 and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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