Taiwan FDA registration 3cb21b6f8b7d7d67e099a51dfeec5816

Lumipulse G BNP

TW: 錄秘帕斯GB型利鈉尿胜檢驗試劑
Taiwan flagTaiwan·Risk Class 2·MD·Fujirebio Inc. Sagamihara Facility·Registered Jan 03, 2019 – Jan 03, 2024Expired
Registration details
Analysis ID
3cb21b6f8b7d7d67e099a51dfeec5816
License Form
Ministry of Health Medical Device Import No. 032004
Customs Code
DHA05603200402
Company information
Manufacturer Country
Japan
Authorized Representative
Grand Marquis IVD CO., LTD.
Product details
Intended Use
This product is used with the Para G1200 Chemical Cryometer to quantitatively measure B-type natriuretic urinalysis (BNP) in plasma.
Product Type (Level 1)
A Clinical chemistry and clinical toxicology
Product Type (Level 2)
A1117 Type B sodium urine peptide test system
Import Information
Imported from abroad
Dates and status
Registration Date
Jan 03, 2019
Expiry Date
Jan 03, 2024
Companies making similar products

Top companies providing products similar to "Lumipulse G BNP"

Recent registrations

Recently registered similar products

About this record

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.

Free DatabasePowered by Pure Global AI89,000+ Devices1 Competitors1 Recent Registrations