Taiwan FDA registration cfc5cf5c9d86a102a4e6bd5c90516f5b

"Rago" blood collection needle (sterile)

TW: "羅碁" 採血針 (滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.;; 羅碁生化科技股份有限公司·Registered May 28, 2015 – May 28, 2025Expired

Registration details

Analysis ID: cfc5cf5c9d86a102a4e6bd5c90516f5b
Customs Code: DHA09600241005

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.;; 羅碁生化科技股份有限公司
Manufacturer Country: Taiwan, Province of China;;China
Authorized Representative: EBIOLOGIC TECHNOLOGY CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: Chinese goods;; Contract manufacturing;; Input;; QMS/QSD

Dates and status

Registration Date: May 28, 2015
Expiry Date: May 28, 2025

About this record

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..

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