Taiwan FDA registration 2fc33e86da3e9fb17d928809fa27e6eb
Bionic complement 4 reagent
TW: 生研補體4試劑
Taiwan·Risk Class 2·DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY·Registered Oct 25, 2005 – Oct 25, 2020CancelledRegistration details
- Analysis ID
- 2fc33e86da3e9fb17d928809fa27e6eb
- Customs Code
- DHA00601323903
Company information
- Manufacturer
- DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY
- Manufacturer Country
- Japan
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- The measure of the turbidity of Supplement 4 (C4) in the serum.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- import
Dates and status
- Registration Date
- Oct 25, 2005
- Expiry Date
- Oct 25, 2020
- Cancellation Date
- Aug 25, 2020
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Bionic complement 4 reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 2fc33e86da3e9fb17d928809fa27e6eb and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.
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