Taiwan FDA registration eea612f50818a461716bab333fb4b7cb
Konya conjugated globulin reagent (unsterilized)
TW: 科尼亞結合球蛋白試劑(未滅菌)
Taiwan·Risk Class 1·KAMIYA BIOMEDICAL COMPANY·Registered Oct 18, 2005 – Oct 18, 2025CancelledRegistration details
- Analysis ID
- eea612f50818a461716bab333fb4b7cb
- Customs Code
- DHA04400100702
Company information
- Manufacturer
- KAMIYA BIOMEDICAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- This measurement is useful in diagnosing heme-binding globulin formation associated with hemolytic disorders (rupture of red blood cells and release of heme) and certain kidney diseases.
- Product Type (Level 1)
- C Immunology and microbiology
- Import Information
- Domestic
Dates and status
- Registration Date
- Oct 18, 2005
- Expiry Date
- Oct 18, 2025
- Cancellation Date
- Jun 30, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷
About this record
Access comprehensive regulatory information for Konya conjugated globulin 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 eea612f50818a461716bab333fb4b7cb and manufactured by KAMIYA BIOMEDICAL COMPANY. 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