Taiwan FDA registration 6d1a3deefb58d8352a95e8b54de20ab4

"Lianxiang" blood lancet (sterilized)

TW: "連陞" 採血針 (滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Nov 16, 2017 – Nov 16, 2027Active

Registration details

Analysis ID: 6d1a3deefb58d8352a95e8b54de20ab4
Customs Code: DHA09600327109

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: LEISON BIOTECH 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: QMS/QSD;; Chinese goods;; input

Dates and status

Registration Date: Nov 16, 2017
Expiry Date: Nov 16, 2027

About this record

Access comprehensive regulatory information for "Lianxiang" 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 6d1a3deefb58d8352a95e8b54de20ab4 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is LEISON BIOTECH CO., LTD..

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