Taiwan FDA registration d12927612bda0f03a92fd0f75124a105

Fore Diamond Lancet (unsterilized)

TW: 福爾鑽石採血筆(未滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jun 05, 2019 – Jun 05, 2024Expired

Registration details

Analysis ID: d12927612bda0f03a92fd0f75124a105
Customs Code: DHA09600382602

Company information

Manufacturer: SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: TAIDOC TECHNOLOGY 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: Chinese goods;; input

Dates and status

Registration Date: Jun 05, 2019
Expiry Date: Jun 05, 2024

About this record

Access comprehensive regulatory information for Fore Diamond Lancet (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d12927612bda0f03a92fd0f75124a105 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

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