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"Bexister" uric acid detection reagent (sterilized) - Taiwan Registration e40e999f7d324fe7401518783afce8fb

Access comprehensive regulatory information for "Bexister" uric acid detection reagent (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number e40e999f7d324fe7401518783afce8fb and manufactured by BIOSYSTEMS S.A.. The authorized representative in Taiwan is HONEST MEDICAL INC..

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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e40e999f7d324fe7401518783afce8fb
Registration Details
Taiwan FDA Registration: e40e999f7d324fe7401518783afce8fb
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Device Details

"Bexister" uric acid detection reagent (sterilized)
TW: "็™พๅธŒๆ–ฏ็‰น" ๅฐฟ้…ธๆชขๆธฌ่ฉฆๅŠ‘ (ๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

e40e999f7d324fe7401518783afce8fb

DHA09401344802

Company Information

Spain

Product Details

Limited to the first level identification range of the "uric acid test system (A.1775)" of the Measures for the Administration of Medical Devices.

A Clinical chemistry and clinical toxicology

A.1775 ๅฐฟ้…ธ่ฉฆ้ฉ—็ณป็ตฑ

Input;; QMS/QSD

Dates and Status

Sep 25, 2013

Sep 25, 2018

Jun 22, 2022

Cancellation Information

Logged out

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