Taiwan FDA registration f99ba4bde340086da8a029bb4e1d718f
Titan III acetate tablets (unsterilized)
TW: 泰坦三代醋酸纖維片(未滅菌)
Taiwan·Risk Class 1·HELENA LABORATORIES CORP.·Registered Nov 16, 2005 – Nov 16, 2025CancelledRegistration details
- Analysis ID
- f99ba4bde340086da8a029bb4e1d718f
- Customs Code
- DHA04400197401
Company information
- Manufacturer
- HELENA LABORATORIES CORP.
- Manufacturer Country
- United States
- Authorized Representative
- SHANG LI INSTRUMENTS CO., LTD.
Product details
- Intended Use
- Different items can be measured with different buffers and color solutions
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.2485 Electrophoresis equipment for clinical use
- Import Information
- import
Dates and status
- Registration Date
- Nov 16, 2005
- Expiry Date
- Nov 16, 2025
- Cancellation Date
- Sep 30, 2021
Cancellation information
- Status
- Logged out
- Reason
- 轉為登錄字號
About this record
Access comprehensive regulatory information for Titan III acetate tablets (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f99ba4bde340086da8a029bb4e1d718f and manufactured by HELENA LABORATORIES CORP.. The authorized representative in Taiwan is SHANG LI INSTRUMENTS CO., LTD..
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