Taiwan FDA registration ae01787a0167e38e4b14c056e29021e1

"Shiheng" surgical instruments, motors and accessories or accessories (unsterilized)

TW: “世亨”手術用器具馬達與配件或附件(未滅菌)

Taiwan·Risk Class 1·SHI HENG TECHNOLOGY CO., LTD.·Registered Aug 24, 2010 – Aug 24, 2025Expired

Registration details

Analysis ID: ae01787a0167e38e4b14c056e29021e1

Company information

Manufacturer: SHI HENG TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: SHI HENG TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Classification and Grading of Medical Devices "Surgical Instruments, Motors and Accessories or Accessories (I.4820)".
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4820 Surgical Appliances and Accessories or Accessories
Import Information: Domestic

Dates and status

Registration Date: Aug 24, 2010
Expiry Date: Aug 24, 2025

About this record

Access comprehensive regulatory information for "Shiheng" surgical instruments, motors and accessories or accessories (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number ae01787a0167e38e4b14c056e29021e1 and manufactured by SHI HENG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is SHI HENG TECHNOLOGY CO., LTD..

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.