Taiwan FDA registration 5afcc00acd31ef4ebd79d27827112f1a

"Weiren" blood lancet (sterilized)

TW: "偉任" 採血針 (滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jul 02, 2018 – Jul 02, 2028Active

Registration details

Analysis ID: 5afcc00acd31ef4ebd79d27827112f1a
Customs Code: DHA09600347308

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: WELLAN TECH 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: Input;; Chinese goods

Dates and status

Registration Date: Jul 02, 2018
Expiry Date: Jul 02, 2028

About this record

Access comprehensive regulatory information for "Weiren" 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 5afcc00acd31ef4ebd79d27827112f1a and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is WELLAN TECH CO., LTD..

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