Taiwan FDA registration 99cdf03df1d4b1c4f3db62264f11e4b4

"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·WUHAN JIN PU MAN BIOTECH CO., LTD·Registered Sep 20, 2017 – Sep 20, 2022Cancelled
Registration details
Analysis ID
99cdf03df1d4b1c4f3db62264f11e4b4
Customs Code
DHA09600322400
Company information
Manufacturer Country
China
Authorized Representative
Siloam Biotech Co., Ltd.
Product details
Intended Use
Limited to the first level identification range of the Measures for the Administration of Medical Devices "Mycoplasma Serological 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
Input;; Chinese goods
Dates and status
Registration Date
Sep 20, 2017
Expiry Date
Sep 20, 2022
Cancellation Date
Apr 12, 2024
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 "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 99cdf03df1d4b1c4f3db62264f11e4b4 and manufactured by WUHAN JIN PU MAN 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 HANGZHOU ALLTEST 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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