Taiwan FDA registration 9c90e2262c266958f18026a749673f94

"Ruikang" blood collection pen (unsterilized)

TW: "睿康" 採血筆 (未滅菌)

Taiwan·Risk Class 1·Ruikang Biomedical Co., Ltd. Precision Factory·Registered Nov 25, 2014 – Nov 25, 2029Active

Registration details

Analysis ID: 9c90e2262c266958f18026a749673f94

Company information

Manufacturer: Ruikang Biomedical Co., Ltd. Precision Factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: MEDIFUN CORPORATION

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: QMS/QSD;; 委託製造;; 國產

Dates and status

Registration Date: Nov 25, 2014
Expiry Date: Nov 25, 2029

About this record

Access comprehensive regulatory information for "Ruikang" blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9c90e2262c266958f18026a749673f94 and manufactured by Ruikang Biomedical Co., Ltd. Precision Factory. The authorized representative in Taiwan is MEDIFUN CORPORATION.

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