Taiwan FDA registration b6897bf2e597b5644105c54ce5ffa366

"Med" hydrogen concentration analyzer (unsterilized)

TW: "麥德" 氫氣濃度分析儀 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD Diagnostics Ltd·Registered Dec 11, 2023 – Dec 11, 2028Active
Registration details
Analysis ID
b6897bf2e597b5644105c54ce5ffa366
Customs Code
DHA09402333801
Company information
Manufacturer
MD Diagnostics Ltd
Manufacturer Country
United Kingdom
Authorized Representative
SHIN CHEN INSTRUMENT CO., LTD.
Product details
Intended Use
Limited to the first level of identification scope of the "Xylose Test System (A.1820)" of the management measures for the classification and grading of medical devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.1820 木糖試驗系統
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Dec 11, 2023
Expiry Date
Dec 11, 2028
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About this record

Access comprehensive regulatory information for "Med" hydrogen concentration analyzer (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number b6897bf2e597b5644105c54ce5ffa366 and manufactured by MD Diagnostics Ltd. The authorized representative in Taiwan is SHIN CHEN INSTRUMENT CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MD DIAGNOSTICS 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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