Taiwan FDA registration c040c0d8307f9404c2f1285d9a026417

Combi Automated Urine Analyzer (Unsterilized)

TW: 康比自動尿液分析儀(未滅菌)
Taiwan flagTaiwan·Risk Class 1·ANALYTICON BIOTECHNOLOGIES AG·Registered Aug 21, 2019 – Aug 21, 2024Cancelled
Registration details
Analysis ID
c040c0d8307f9404c2f1285d9a026417
Customs Code
DHA09402078202
Company information
Manufacturer Country
Germany
Authorized Representative
IN FUNG CO., LTD.
Product details
Intended Use
Limited to the first level identification range of the "Automatic Urinalysis System (A.2900)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.2900 Automated urinalysis system
Import Information
QMS/QSD;; 輸入
Dates and status
Registration Date
Aug 21, 2019
Expiry Date
Aug 21, 2024
Cancellation Date
Sep 30, 2021
Cancellation information
Status
Logged out
Reason
轉為登錄字號
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About this record

Access comprehensive regulatory information for Combi Automated Urine 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 c040c0d8307f9404c2f1285d9a026417 and manufactured by ANALYTICON BIOTECHNOLOGIES AG. The authorized representative in Taiwan is IN FUNG CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including ANALYTICON BIOTECHNOLOGIES AG, 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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