Taiwan FDA registration ad1076dc35d79a106dad438559eb372d

"Yifan Continuous" Heel Blood Collection Device (Sterilization)

TW: "醫凡連發" 腳跟採血器(滅菌)

Taiwan·Risk Class 1·Shandong Lianfa Medical Plastic Products Co., Ltd·Registered Jul 23, 2024 – Jul 23, 2029Active

Registration details

Analysis ID: ad1076dc35d79a106dad438559eb372d
Customs Code: DHA09600496508

Company information

Manufacturer: Shandong Lianfa Medical Plastic Products Co., Ltd
Manufacturer Country: China
Authorized Representative: EAFAN ENTERPRISE CO., LTD.

Product details

Intended Use: It is limited to the first level of identification scope of the "General Surgical Manual Instruments (I.4800)" of the Measures for the Classification and Grading of Medical Devices.
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: Jul 23, 2024
Expiry Date: Jul 23, 2029

About this record

Access comprehensive regulatory information for "Yifan Continuous" Heel Blood Collection Device (Sterilization) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ad1076dc35d79a106dad438559eb372d and manufactured by Shandong Lianfa Medical Plastic Products Co., Ltd. The authorized representative in Taiwan is EAFAN ENTERPRISE CO., LTD..

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