Taiwan FDA registration 1ba162892570212736cb27902b66bdf6
Konya lipoprotein element AI reagent (unsterilized)
TW: 科尼亞脂蛋白元 AI 試劑(未滅菌)
Taiwan·Risk Class 1·KAMIYA BIOMEDICAL COMPANY·Registered Aug 30, 2006 – Aug 30, 2021CancelledRegistration details
- Analysis ID
- 1ba162892570212736cb27902b66bdf6
- Customs Code
- DHA04400510101
Company information
- Manufacturer
- KAMIYA BIOMEDICAL COMPANY
- Manufacturer Country
- United States
- Authorized Representative
- TUNYEN ENTERPRISE CORPORATION
Product details
- Intended Use
- Limited to the first level recognition range of the lipoprotein test system (A.1475) of the medical device management method.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1475 Lipoprotein Testing System
- Import Information
- import
Dates and status
- Registration Date
- Aug 30, 2006
- Expiry Date
- Aug 30, 2021
- Cancellation Date
- Jun 30, 2022
Cancellation information
- Status
- Logged out
- Reason
- 自請註銷;;屆期未申請展延
About this record
Access comprehensive regulatory information for Konya lipoprotein element AI 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 1ba162892570212736cb27902b66bdf6 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