Taiwan FDA registration 8cafbaf1ebfdd4a7f2ce2dc92f665a68

"Lianhua" blood lancet (unsterilized)

TW: "聯珐"採血針(未滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD·Registered Jul 04, 2018 – Jul 04, 2023Expired

Registration details

Analysis ID: 8cafbaf1ebfdd4a7f2ce2dc92f665a68
Customs Code: DHA09600347805

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 Measures for the Administration of Medical Devices "Manual Instruments for General Surgery (I.4800)".
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: Jul 04, 2018
Expiry Date: Jul 04, 2023

About this record

Access comprehensive regulatory information for "Lianhua" blood 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 8cafbaf1ebfdd4a7f2ce2dc92f665a68 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD. The authorized representative in Taiwan is BEAM INTERNATIONAL INC..

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