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Xiec anti-cyclic citrullinated IgG antibody reagent - Taiwan Registration f88325cca0e4fd61f62b7704eb5f73cb

Access comprehensive regulatory information for Xiec anti-cyclic citrullinated IgG antibody reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f88325cca0e4fd61f62b7704eb5f73cb and manufactured by EUROIMMUN MEDIZINISCHE LABORDIAGNOSTIKA AG. The authorized representative in Taiwan is SEEKERS BIOMEDICAL CO., LTD..

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f88325cca0e4fd61f62b7704eb5f73cb
Registration Details
Taiwan FDA Registration: f88325cca0e4fd61f62b7704eb5f73cb
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Device Details

Xiec anti-cyclic citrullinated IgG antibody reagent
TW: ๅ”ๅ…‹ๆŠ—็’ฐ็“œๆฐจ้…ธIgGๆŠ—้ซ”่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

f88325cca0e4fd61f62b7704eb5f73cb

DHA00602335103

Company Information

Product Details

This ELISA test group provides half quantitative or quantitative in vitro assays to determine human autoantibodies to IgG against cyclic citrullinated peptide (CCP).

C Immunology and microbiology

C.5775 ้กž้ขจๆฟ•ๆ€งๅ› ๅญๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Mar 14, 2012

Mar 14, 2022

Apr 12, 2024

Cancellation Information

Logged out

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