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Recording of Paz G Fetal Protein-N Test Reagent Standard - Taiwan Registration 310e00cad0be4de9dc0c2343079971e9

Access comprehensive regulatory information for Recording of Paz G Fetal Protein-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 310e00cad0be4de9dc0c2343079971e9 and manufactured by Fujirebio Inc. Sagamihara Facility. The authorized representative in Taiwan is Grand Marquis IVD CO., LTD..

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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310e00cad0be4de9dc0c2343079971e9
Registration Details
Taiwan FDA Registration: 310e00cad0be4de9dc0c2343079971e9
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Device Details

Recording of Paz G Fetal Protein-N Test Reagent Standard
TW: ้Œ„็ง˜ๅธ•ๆ–ฏG็”ฒๅž‹่ƒŽๅ…’่›‹็™ฝ-Nๆชข้ฉ—่ฉฆๅŠ‘ๆจ™ๆบ–ๆถฒ
Risk Class 2

Registration Details

310e00cad0be4de9dc0c2343079971e9

DHA00602193608

Company Information

Product Details

Calibration reagent specially used to record the detection reagent of Paz G Fetal Protein-N

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Jan 10, 2011

Jan 10, 2026