Taiwan FDA registration 10aa06f01c96ae62a8f0049c9ffd5478

"Omon automatic western blotting instrument"

TW: “歐蒙” 全自動免疫印跡儀
Taiwan flagTaiwan·Risk Class 2·EUROIMMUN (HANGZHOU) MEDICAL LABORATORY DIAGNOSTICS CO., LTD.·Registered Feb 02, 2021 – Feb 02, 2026Expired
Registration details
Analysis ID
10aa06f01c96ae62a8f0049c9ffd5478
Customs Code
DHA09200103102
Company information
Manufacturer Country
China
Product details
Intended Use
This product adopts immunoblotting method (Oumeng blot method), which is used together with supporting detection reagents to detect specific antigens or antibodies in human serum or plasma samples, and realize the automatic operation of dosing, liquid addition, incubation, cleaning, air drying, and digital image acquisition and analysis of membrane strips.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A.9999 Miscellaneous  
Import Information
Input;; Chinese goods
Dates and status
Registration Date
Feb 02, 2021
Expiry Date
Feb 02, 2026
About this record

Access comprehensive regulatory information for "Omon automatic western blotting instrument" in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 10aa06f01c96ae62a8f0049c9ffd5478 and manufactured by EUROIMMUN (HANGZHOU) MEDICAL LABORATORY DIAGNOSTICS CO., LTD.. The authorized representative in Taiwan is EUROIMMUN (SOUTH EAST ASIA) PTE. LTD. TAIWAN BRANCH (SINGAPORE).

This page provides complete technical specifications, regulatory compliance details. 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.

Free DatabasePowered by Pure Global AI89,000+ Devices