Taiwan FDA registration a7a9723e6d1d049d29b9a2ffc0c9dabd
Guofa Smear Kit (Unsterilized)
TW: 國發抹片組合包(未滅菌)
Registration details
- Analysis ID
- a7a9723e6d1d049d29b9a2ffc0c9dabd
- Customs Code
- DHY04300130809
Company information
- Manufacturer
- K.F. MEDICAL INSTRUMENTS CO., LTD.
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- K.F. MEDICAL INSTRUMENTS CO., LTD.
Product details
- Product Type (Level 1)
- C Immunology and microbiology
- Product Type (Level 2)
- C.2900 Microbial sample collection and delivery equipment
- Import Information
- Domestic
Dates and status
- Registration Date
- Apr 21, 2006
- Expiry Date
- Apr 21, 2026
About this record
Access comprehensive regulatory information for Guofa Smear Kit (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number a7a9723e6d1d049d29b9a2ffc0c9dabd and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS 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