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Bioken Immunosphere Protein M Tester - Taiwan Registration 7d117bfcedfe5f2d21680e69ccc40190

Access comprehensive regulatory information for Bioken Immunosphere Protein M Tester in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 7d117bfcedfe5f2d21680e69ccc40190 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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7d117bfcedfe5f2d21680e69ccc40190
Registration Details
Taiwan FDA Registration: 7d117bfcedfe5f2d21680e69ccc40190
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Device Details

Bioken Immunosphere Protein M Tester
TW: ็”Ÿ็ ”ๅ…็–ซ็ƒ่›‹็™ฝM่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

7d117bfcedfe5f2d21680e69ccc40190

DHA00601317901

Company Information

Product Details

Measure the level of immunoglobulin M (IgM) in serum.

C Immunology and microbiology

import

Dates and Status

Oct 14, 2005

Oct 14, 2020

Aug 18, 2020

Cancellation Information

Logged out

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