Taiwan FDA registration 8fd218f805d5dec0f4f99be06ef98e1e

"Lotus hair" blood collection pen (unsterilized)

TW: "蓮發" 採血筆 (未滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jun 03, 2019 – Jun 03, 2029Active

Registration details

Analysis ID: 8fd218f805d5dec0f4f99be06ef98e1e
Customs Code: DHA09600382309

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: YEHSHANG ENTERPRISE CORPORATION

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: Jun 03, 2019
Expiry Date: Jun 03, 2029

About this record

Access comprehensive regulatory information for "Lotus hair" 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 8fd218f805d5dec0f4f99be06ef98e1e and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is YEHSHANG ENTERPRISE CORPORATION.

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