Taiwan FDA registration 7ac898b52f2a19ab40a75935a9d4ce55

"Wei Ren" blood collection pen (unsterilized)

TW: "偉任" 採血筆 (未滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Dec 28, 2018 – Dec 28, 2028Active

Registration details

Analysis ID: 7ac898b52f2a19ab40a75935a9d4ce55
Customs Code: DHA09600365106

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: Chinese goods;; input

Dates and status

Registration Date: Dec 28, 2018
Expiry Date: Dec 28, 2028

About this record

Access comprehensive regulatory information for "Wei Ren" 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 7ac898b52f2a19ab40a75935a9d4ce55 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is WELLAN TECH CO., LTD..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.