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"Oumon" automatic western blotting instrument - Taiwan Registration b1ea3860718b8863a67cdb828b5ba1ff

Access comprehensive regulatory information for "Oumon" 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 b1ea3860718b8863a67cdb828b5ba1ff and manufactured by DYNEX TECHNOLOGIES, SPOL. S.R.O.; EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. 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.

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b1ea3860718b8863a67cdb828b5ba1ff
Registration Details
Taiwan FDA Registration: b1ea3860718b8863a67cdb828b5ba1ff
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Device Details

"Oumon" automatic western blotting instrument
TW: "ๆญ่’™"ๅ…จ่‡ชๅ‹•ๅ…็–ซๅฐ่ทกๅ„€
Risk Class 2

Registration Details

b1ea3860718b8863a67cdb828b5ba1ff

DHA05603368100

Product Details

This product is a fully automated instrument for processing EUROIMMUN western blot tests (Western blot and EUROLINE).

A Clinical chemistry and clinical toxicology

A.9999 Miscellaneous ใ€€

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Dates and Status

Sep 25, 2020

Sep 25, 2025