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RIDASCREEN Haemoglobin - Taiwan Registration 605cfe5eb131d2e23c9cd8786cc2f52d

Access comprehensive regulatory information for RIDASCREEN Haemoglobin in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 605cfe5eb131d2e23c9cd8786cc2f52d and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is METEK LAB 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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605cfe5eb131d2e23c9cd8786cc2f52d
Registration Details
Taiwan FDA Registration: 605cfe5eb131d2e23c9cd8786cc2f52d
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Device Details

RIDASCREEN Haemoglobin
TW: ็‘ž้”็ณžไพฟๆฝ›่ก€่ก€็ด…็ด ๆชขๆธฌๅฅ—็ต„
Risk Class 2
MD
Cancelled

Registration Details

605cfe5eb131d2e23c9cd8786cc2f52d

Ministry of Health Medical Device Import No. 025845

DHA05602584505

Company Information

Germany

Product Details

B Hematology and pathology devices

B6550 Occult blood test

Imported from abroad

Dates and Status

Jan 07, 2014

Jan 07, 2024

Jan 10, 2020

Cancellation Information

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