Taiwan FDA registration aacb5564f8df8d74e3730fb3c31855f6

"Apricot Whole" blood collection needle (sterilized)

TW: "杏全"採血針(滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Apr 22, 2019 – Apr 22, 2029Active

Registration details

Analysis ID: aacb5564f8df8d74e3730fb3c31855f6
Customs Code: DHA09600375900

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: BEAM INTERNATIONAL INC.

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: QMS/QSD;; Chinese goods;; input

Dates and status

Registration Date: Apr 22, 2019
Expiry Date: Apr 22, 2029

About this record

Access comprehensive regulatory information for "Apricot Whole" 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 aacb5564f8df8d74e3730fb3c31855f6 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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