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"Rago" blood collection needle (sterile) - Taiwan Registration cfc5cf5c9d86a102a4e6bd5c90516f5b

Access comprehensive regulatory information for "Rago" blood collection needle (sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cfc5cf5c9d86a102a4e6bd5c90516f5b and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.;; 羅碁生化科技股份有限公司. The authorized representative in Taiwan is EBIOLOGIC TECHNOLOGY 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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cfc5cf5c9d86a102a4e6bd5c90516f5b
Registration Details
Taiwan FDA Registration: cfc5cf5c9d86a102a4e6bd5c90516f5b
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Device Details

"Rago" blood collection needle (sterile)
TW: "羅碁" 採血針 (滅菌)
Risk Class 1

Registration Details

cfc5cf5c9d86a102a4e6bd5c90516f5b

DHA09600241005

Company Information

Product Details

Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.

I General, Plastic Surgery and Dermatology

I.4800 Hand Instruments for General Surgery

Chinese goods;; Contract manufacturing;; Input;; QMS/QSD

Dates and Status

May 28, 2015

May 28, 2025