Taiwan FDA registration 45cb66deda6651e94481eb77421c2ddf

"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 Mar 10, 2017 – Mar 10, 2022Cancelled
Registration details
Analysis ID
45cb66deda6651e94481eb77421c2ddf
Customs Code
DHA09401759009
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 identification range of the Xylose Test System (A.1820) of the Measures for the Administration 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
Mar 10, 2017
Expiry Date
Mar 10, 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 "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 45cb66deda6651e94481eb77421c2ddf 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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