Taiwan FDA registration f002c28601d54ae98e9e6f151be194af

"Pushen" progesterone test reagent (unsterilized)

TW: "普生" 黃體脂酮檢驗試劑(未滅菌)
Taiwan flagTaiwan·Risk Class 1·GENERAL BIOLOGICALS CORP.·Registered Jun 04, 2014 – Jun 04, 2024Expired
Registration details
Analysis ID
f002c28601d54ae98e9e6f151be194af
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
GENERAL BIOLOGICALS CORP.
Product details
Intended Use
Limited to the first level of identification scope of the progesterone test system (A.1620) of the classification and grading management measures for medical devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1620 Progesterone testing system
Import Information
Domestic
Dates and status
Registration Date
Jun 04, 2014
Expiry Date
Jun 04, 2024
Companies making similar products

Top companies providing products similar to ""Pushen" progesterone test reagent (unsterilized)"

Recent registrations

Recently registered similar products

About this record

Access comprehensive regulatory information for "Pushen" progesterone 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 f002c28601d54ae98e9e6f151be194af and manufactured by GENERAL BIOLOGICALS CORP.. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including GENERAL BIOLOGICALS CORP., and 1 recent registrations in the same category. 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+ Devices1 Competitors1 Recent Registrations