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Bioresearch liquid correction solution - Taiwan Registration 887c0f6bf3c4607e9768eb774a53adf4

Access comprehensive regulatory information for Bioresearch liquid correction solution in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 887c0f6bf3c4607e9768eb774a53adf4 and manufactured by DENKA SEIKEN CO., LTD. KAGAMIDA FACTORY. The authorized representative in Taiwan is TUNYEN ENTERPRISE CORPORATION.

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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887c0f6bf3c4607e9768eb774a53adf4
Registration Details
Taiwan FDA Registration: 887c0f6bf3c4607e9768eb774a53adf4
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Device Details

Bioresearch liquid correction solution
TW: ็”Ÿ็ ”ๆถฒ็‹€ๆ กๆญฃๆถฒ
Risk Class 2
Cancelled

Registration Details

887c0f6bf3c4607e9768eb774a53adf4

DHA00601569704

Company Information

Product Details

It is used to establish a reference point in the test reagent to determine the measured value of the substance in the human sample.

A Clinical chemistry and clinical toxicology

A.1150 Calibrated Products

import

Dates and Status

Dec 20, 2005

Dec 20, 2025

Jul 07, 2022

Cancellation Information

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