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Recording of Paz G carcinoembryonic antigen-N test reagent standard - Taiwan Registration f9c17a21e238c060ebb6016caddaa621

Access comprehensive regulatory information for Recording of Paz G carcinoembryonic antigen-N test reagent standard in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number f9c17a21e238c060ebb6016caddaa621 and manufactured by Fujirebio Inc. Sagamihara Facility. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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f9c17a21e238c060ebb6016caddaa621
Registration Details
Taiwan FDA Registration: f9c17a21e238c060ebb6016caddaa621
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Device Details

Recording of Paz G carcinoembryonic antigen-N test reagent standard
TW: ้Œ„็ง˜ๅธ•ๆ–ฏG็™Œ่ƒšๆŠ—ๅŽŸ-Nๆชข้ฉ—่ฉฆๅŠ‘ๆจ™ๆบ–ๆถฒ
Risk Class 2

Registration Details

f9c17a21e238c060ebb6016caddaa621

DHA00602196005

Company Information

Product Details

Calibration reagent specially used to record Paz G carcinoembryonic antigen-N detection reagent.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Mar 14, 2011

Mar 14, 2026