Taiwan FDA registration db19d189a143beefd803ca8a86c72495

"Taibo Burst" blood collection pen (unsterilized)

TW: "泰博連發"採血筆(未滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Mar 08, 2019 – Mar 08, 2029Active

Registration details

Analysis ID: db19d189a143beefd803ca8a86c72495
Customs Code: DHA09600371200

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: Mar 08, 2019
Expiry Date: Mar 08, 2029

About this record

Access comprehensive regulatory information for "Taibo Burst" blood collection pen (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number db19d189a143beefd803ca8a86c72495 and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is TAIDOC TECHNOLOGY CORPORATION.

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