Taiwan FDA registration 300e000678bd5ea9fdc236101201f416

Fukunaga continuous blood collection needle (sterilized)

TW: 福永連發採血針(滅菌)

Taiwan·Risk Class 1·Shandong Lianfa Medical Plastic Products Co., Ltd.·Registered Oct 15, 2019 – Oct 15, 2029Active

Registration details

Analysis ID: 300e000678bd5ea9fdc236101201f416
Customs Code: DHA09600398904

Company information

Manufacturer: Shandong Lianfa Medical Plastic Products Co., Ltd.
Manufacturer Country: China
Authorized Representative: EPS BIO TECHNOLOGY CORP.

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;; QMS/QSD

Dates and status

Registration Date: Oct 15, 2019
Expiry Date: Oct 15, 2029

About this record

Access comprehensive regulatory information for Fukunaga continuous blood collection needle (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 300e000678bd5ea9fdc236101201f416 and manufactured by Shandong Lianfa Medical Plastic Products Co., Ltd.. The authorized representative in Taiwan is EPS BIO TECHNOLOGY CORP..

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