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Bofang allergen detection reagent No. 1 - Taiwan Registration cba2af397cb0f4decba8c128ca66a746

Access comprehensive regulatory information for Bofang allergen detection reagent No. 1 in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number cba2af397cb0f4decba8c128ca66a746 and manufactured by R-BIOPHARM AG. The authorized representative in Taiwan is IN FUNG CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including R-BIOPHARM AG, 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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Registration Details
Taiwan FDA Registration: cba2af397cb0f4decba8c128ca66a746
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Device Details

Bofang allergen detection reagent No. 1
TW: ไผฏๆ–น้Žๆ•ๅŽŸๆชขๆธฌ่ฉฆๅŠ‘1่™Ÿ
Risk Class 2
Cancelled

Registration Details

cba2af397cb0f4decba8c128ca66a746

DHA00602152806

Company Information

Germany

Product Details

It is an in vitro diagnostic reagent. This is an enzyme immunosorbent assay that uses nitrocellulose membrane to detect specific immunoglobulin E antibodies produced against endemic allergens in human serum.

C Immunology and microbiology

C.5510 ๅ…็–ซ็ƒ่›‹็™ฝA,G,M,DๅŠEๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Sep 09, 2010

Oct 18, 2020

May 19, 2022

Cancellation Information

Logged out

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