Taiwan FDA registration 2e12111de16bf38c2343954b9cfb33bb
"Dechang" ovulation reagent
TW: "迪昌" 排卵試劑
Registration details
- Analysis ID
- 2e12111de16bf38c2343954b9cfb33bb
- Customs Code
- DHA04600013901
Company information
- Manufacturer
- RUNBIO BIOTECH CO., LTD.
- Manufacturer Country
- China
- Authorized Representative
- Dechang Pharmaceutical Co., Ltd
Product details
- Intended Use
- The amount and changes of luteinizing in the urine of women were measured.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1485 Progesterone testing system
- Import Information
- import
Dates and status
- Registration Date
- Mar 27, 2006
- Expiry Date
- Dec 05, 2008
- Cancellation Date
- Jan 19, 2009
Cancellation information
- Status
- Logged out
- Reason
- 公司歇業
About this record
Access comprehensive regulatory information for "Dechang" ovulation reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2e12111de16bf38c2343954b9cfb33bb and manufactured by RUNBIO BIOTECH CO., LTD.. The authorized representative in Taiwan is Dechang Pharmaceutical 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.
Free DatabasePowered by Pure Global AI89,000+ Devices