Taiwan FDA registration 9f011a9a08e2bf446b4483ddcb28cbf4

"Lexia" blood collection needle (sterilization)

TW: “樂協”採血針(滅菌)

Taiwan·Risk Class 1·Shandong Lianfa Medical Plastic Products Co., Ltd.·Registered Oct 15, 2020 – Oct 15, 2025Expired

Registration details

Analysis ID: 9f011a9a08e2bf446b4483ddcb28cbf4
Customs Code: DHA09600433807

Company information

Manufacturer: Shandong Lianfa Medical Plastic Products Co., Ltd.
Manufacturer Country: China
Authorized Representative: LUVNSHARE BIOMEDICAL, 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: Chinese goods;; Input;; QMS/QSD

Dates and status

Registration Date: Oct 15, 2020
Expiry Date: Oct 15, 2025

About this record

Access comprehensive regulatory information for "Lexia" blood collection needle (sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 9f011a9a08e2bf446b4483ddcb28cbf4 and manufactured by Shandong Lianfa Medical Plastic Products Co., Ltd.. The authorized representative in Taiwan is LUVNSHARE BIOMEDICAL, INC..

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