Taiwan FDA registration a62ee12a0567ce6f59af661cf831ef64

"Lexia" blood collection pen (unsterilized)

TW: “樂協”採血筆(未滅菌)

Taiwan·Risk Class 1·Shandong Lianfa Medical Plastic Products Co., Ltd.·Registered Oct 16, 2020 – Oct 16, 2025Expired

Registration details

Analysis ID: a62ee12a0567ce6f59af661cf831ef64
Customs Code: DHA09600434109

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: Input;; Chinese goods;; QMS/QSD

Dates and status

Registration Date: Oct 16, 2020
Expiry Date: Oct 16, 2025

About this record

Access comprehensive regulatory information for "Lexia" 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 a62ee12a0567ce6f59af661cf831ef64 and manufactured by Shandong Lianfa Medical Plastic Products Co., Ltd.. The authorized representative in Taiwan is LUVNSHARE BIOMEDICAL, INC..

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