Taiwan FDA registration 63d72c09e6e636c60d0c902857ccac9d

"Lianxian" blood collection pen (unsterilized)

TW: "連陞" 採血筆 (未滅菌)

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

Registration details

Analysis ID: 63d72c09e6e636c60d0c902857ccac9d
Customs Code: DHA09600327201

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: Input;; Chinese goods

Dates and status

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

About this record

Access comprehensive regulatory information for "Lianxian" 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 63d72c09e6e636c60d0c902857ccac9d and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is LEISON BIOTECH CO., LTD..

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