Taiwan FDA registration d509321561deed4d4fff2b3ccf1a8058

Pursen-thyroxine radioimmunoassay reagent

TW: 普生甲狀腺素放射免疫分析試劑
Taiwan flagTaiwan·Risk Class 2·MP BIOMEDICALS DIAGNOSTICS DIVISION·Registered Dec 21, 2011 – Dec 21, 2026Active
Registration details
Analysis ID
d509321561deed4d4fff2b3ccf1a8058
Customs Code
DHAS0602306701
Company information
Manufacturer Country
United States
Authorized Representative
GENERAL BIOLOGICALS CORP.
Product details
Intended Use
Quantitatively measure the concentration of total thyroxine (T4) in human serum and plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1700 Total thyroxine 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
Dec 21, 2011
Expiry Date
Dec 21, 2026
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About this record

Access comprehensive regulatory information for Pursen-thyroxine 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 d509321561deed4d4fff2b3ccf1a8058 and manufactured by MP BIOMEDICALS DIAGNOSTICS DIVISION. The authorized representative in Taiwan is GENERAL BIOLOGICALS CORP..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MP BIOMEDICALS, INC., and 1 recent registrations in the same category. 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.

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