Taiwan FDA registration ad328c528e19d34f0b709db3d24097c6

"Xiangguo" retractable needle lancet (unsterilized)

TW: "翔國"可退針式採血筆(未滅菌)

Taiwan·Risk Class 1·JINAN LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.·Registered Oct 25, 2011 – Oct 25, 2021Cancelled

Registration details

Analysis ID: ad328c528e19d34f0b709db3d24097c6
Customs Code: DHA04600149604

Company information

Manufacturer: JINAN LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.
Manufacturer Country: China
Authorized Representative: SCIENCO TECHNOLOGY CORP.

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: import

Dates and status

Registration Date: Oct 25, 2011
Expiry Date: Oct 25, 2021
Cancellation Date: Sep 08, 2023

Cancellation information

Status: Logged out
Reason: 未展延而逾期者

About this record

Access comprehensive regulatory information for "Xiangguo" retractable needle 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 ad328c528e19d34f0b709db3d24097c6 and manufactured by JINAN LIANFA MEDICAL PLASTIC PRODUCTS CO., LTD.. The authorized representative in Taiwan is SCIENCO TECHNOLOGY CORP..

This page provides complete technical specifications, regulatory compliance details. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.