Taiwan FDA registration 87d73cf7e839eed668b5cd9149184fdc

"Alans" lancet (sterilized)

TW: "亞蘭斯" 採血針 (滅菌)

Taiwan·Risk Class 1·SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Jan 10, 2017 – Jan 10, 2022Cancelled

Registration details

Analysis ID: 87d73cf7e839eed668b5cd9149184fdc
Customs Code: DHA09600296600

Company information

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

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: Chinese goods;; input

Dates and status

Registration Date: Jan 10, 2017
Expiry Date: Jan 10, 2022
Cancellation Date: Apr 12, 2024

Cancellation information

Status: Logged out
Reason: 許可證已逾有效期

About this record

Access comprehensive regulatory information for "Alans" lancet (sterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 87d73cf7e839eed668b5cd9149184fdc and manufactured by SHANDONG LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is ALLIANCE INTERNATIONAL MEDICAL CO., LTD..

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