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Speedodine RA test reagent - Taiwan Registration ab29595812690bb555029de513182041

Access comprehensive regulatory information for Speedodine RA test reagent in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ab29595812690bb555029de513182041 and manufactured by FUJIREBIO INC., HACHIOJI FACILITY. The authorized representative in Taiwan is Taiwan Fu Pharmaceutical Co., Ltd.

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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ab29595812690bb555029de513182041
Registration Details
Taiwan FDA Registration: ab29595812690bb555029de513182041
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Device Details

Speedodine RA test reagent
TW: ้€Ÿๆจ‚ๅฎšRAๆชข้ฉ—่ฉฆๅŠ‘
Risk Class 2
Cancelled

Registration Details

ab29595812690bb555029de513182041

DHA00601550801

Company Information

Product Details

ๅˆฉ็”จ่ขซๅ‹•็ฒ’ๅญๅ‡้›†ๆณ•ๆชขๆธฌไบบ่ก€ๆธ…ไธญไน‹Rheumatoid Factor.

C Immunology and microbiology

C.5775 ้กž้ขจๆฟ•ๆ€งๅ› ๅญๅ…็–ซ่ฉฆ้ฉ—็ณป็ตฑ

import

Dates and Status

Dec 13, 2005

Dec 13, 2015

May 17, 2018

Cancellation Information

Logged out

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