Taiwan FDA registration 2707b5b3d5eb60ee689d8efe86070013

Tai Xin disposable blood lancet (sterilized)

TW: 台欣一次性採血針 (滅菌)

Taiwan·Risk Class 1·Shandong Lianfa Medical Plastic Products Co., Ltd.·Registered Aug 29, 2019 – Aug 29, 2029Active

Registration details

Analysis ID: 2707b5b3d5eb60ee689d8efe86070013
Customs Code: DHA09600394204

Company information

Manufacturer: Shandong Lianfa Medical Plastic Products Co., Ltd.
Manufacturer Country: China
Authorized Representative: TYSON BIORESEARCH INC.

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: Input;; QMS/QSD;; Chinese goods

Dates and status

Registration Date: Aug 29, 2019
Expiry Date: Aug 29, 2029

About this record

Access comprehensive regulatory information for Tai Xin disposable blood lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2707b5b3d5eb60ee689d8efe86070013 and manufactured by Shandong Lianfa Medical Plastic Products Co., Ltd.. The authorized representative in Taiwan is TYSON BIORESEARCH INC..

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