Taiwan FDA registration ab245b96bfd981e48196b18fc7e58d2f

Martin Peter Triiodothyroxine radioimmunoassay reagent

TW: 馬丁彼得三碘甲狀腺素放射免疫分析試劑
Taiwan flagTaiwan·Risk Class 2·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Oct 18, 2011 – Oct 18, 2021Cancelled
Registration details
Analysis ID
ab245b96bfd981e48196b18fc7e58d2f
Customs Code
DHAS0602273001
Company information
Manufacturer Country
United States
Authorized Representative
GENERAL BIOLOGICALS CORP.
Product details
Intended Use
The T3 concentration in the serum is tested and the thyroid function is interpreted to determine whether there is a thyroid metabolism problem.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1710 Total triiodothyroxine test system
Import Information
Consent must be attached to the import (with the consent of the Atomic Energy Commission must be obtained for each import); input
Dates and status
Registration Date
Oct 18, 2011
Expiry Date
Oct 18, 2021
Cancellation Date
Aug 15, 2023
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Martin Peter Triiodothyroxine radioimmunoassay reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab245b96bfd981e48196b18fc7e58d2f and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

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