Taiwan FDA registration d4b530ccd9c983cebbf8860959afecd7
Martin Peter Triiodothyroxine Uptake Test Reagent (Unsterilized)
TW: 馬丁彼得三碘甲狀腺素攝取率檢驗試劑(未滅菌)
Taiwan·Risk Class 1·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Sep 12, 2005 – Sep 12, 2020CancelledRegistration details
- Analysis ID
- d4b530ccd9c983cebbf8860959afecd7
- Customs Code
- DHAS4400042201
Company information
- Manufacturer
- MP BIOMEDICALS DIAGNOSTICS DIVISION
- Manufacturer Country
- United States
- Authorized Representative
- GENERAL BIOLOGICALS CORP.
Product details
- Intended Use
- Test the rate of triiodothyrenol in serum.
- Product Type (Level 1)
- A Clinical chemistry and clinical toxicology
- Product Type (Level 2)
- A.1715 Triiodothyroxine absorption test system
- Import Information
- import
Dates and status
- Registration Date
- Sep 12, 2005
- Expiry Date
- Sep 12, 2020
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for Martin Peter Triiodothyroxine Uptake Test 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 d4b530ccd9c983cebbf8860959afecd7 and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..
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