Taiwan FDA registration b5c6ddbdb0be2a540f31acea39c51193

Iron-Soluble Rapid Plasma Reagin Reagent Set

TW: 鐵可快速血漿反應素試劑組
Taiwan flagTaiwan·TECO DIAGNOSTICS·Registered Dec 22, 2005 – Dec 22, 2010Cancelled
Registration details
Analysis ID
b5c6ddbdb0be2a540f31acea39c51193
Customs Code
DHA00601571901
Company information
Manufacturer
TECO DIAGNOSTICS
Manufacturer Country
United States
Authorized Representative
HONEST MEDICAL INC.
Product details
Intended Use
A qualitative and semi-quantitative rapid test for the detection of non-treponemal antibodies to reagin antibodies in human serum and plasma.
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3820 Treponema pallidum non-spirochal test
Import Information
import
Dates and status
Registration Date
Dec 22, 2005
Expiry Date
Dec 22, 2010
Cancellation Date
Nov 01, 2011
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 Iron-Soluble Rapid Plasma Reagin Reagent Set in Taiwan's medical device market through Pure Global AI's free database. is registered under number b5c6ddbdb0be2a540f31acea39c51193 and manufactured by TECO DIAGNOSTICS. The authorized representative in Taiwan is HONEST MEDICAL INC..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including TONYAR BIOTECH. 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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