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Lumipulse G BNP - Taiwan Registration 3cb21b6f8b7d7d67e099a51dfeec5816

Access comprehensive regulatory information for Lumipulse G BNP in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 3cb21b6f8b7d7d67e099a51dfeec5816 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, 1 companies making similar products including FUJIREBIO INC., HACHIOJI FACILITY, and 1 recent registrations in the same category. 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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3cb21b6f8b7d7d67e099a51dfeec5816
Registration Details
Taiwan FDA Registration: 3cb21b6f8b7d7d67e099a51dfeec5816
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Device Details

Lumipulse G BNP
TW: ้Œ„็ง˜ๅธ•ๆ–ฏGBๅž‹ๅˆฉ้ˆ‰ๅฐฟ่ƒœๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2
MD

Registration Details

3cb21b6f8b7d7d67e099a51dfeec5816

Ministry of Health Medical Device Import No. 032004

DHA05603200402

Company Information

Product Details

This product is used with the Para G1200 Chemical Cryometer to quantitatively measure B-type natriuretic urinalysis (BNP) in plasma.

A Clinical chemistry and clinical toxicology

A1117 Type B sodium urine peptide test system

Imported from abroad

Dates and Status

Jan 03, 2019

Jan 03, 2024

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