Taiwan FDA registration 04c642d128d93780799898d74762cf9a

"Siloa" Pneumoniae Mycoplasma Detection Reagent (Unsterilized)

TW: "西羅亞" 肺炎黴漿菌檢測試劑 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·HANGZHOU ALLTEST BIOTECH CO., LTD.·Registered Oct 25, 2019 – Oct 25, 2029Active
Registration details
Analysis ID
04c642d128d93780799898d74762cf9a
Customs Code
DHA09600399805
Company information
Manufacturer Country
China
Authorized Representative
Siloam Biotech Co., Ltd.
Product details
Intended Use
Limited to the classification and grading management method of medical equipment, the first level identification range of "Mycoplasma serum reagent (C.3375)".
Product Type (Level 1)
C Immunology and microbiology
Product Type (Level 2)
C.3375 黴漿菌屬血清試劑
Import Information
Chinese goods;; input
Dates and status
Registration Date
Oct 25, 2019
Expiry Date
Oct 25, 2029
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About this record

Access comprehensive regulatory information for "Siloa" Pneumoniae Mycoplasma Detection 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 04c642d128d93780799898d74762cf9a and manufactured by HANGZHOU ALLTEST BIOTECH CO., LTD.. The authorized representative in Taiwan is Siloam Biotech Co., Ltd..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including WUHAN JIN PU MAN BIOTECH CO., LTD, 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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