Taiwan FDA registration cde2585830f2780b18bfbb58d370ffee

"Huasheng" Speculum and Accessories (Non-Sterile)

TW: "華陞" 檢查鏡及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·HUA SHENG INSTRUMENTS CO., LTD.·Registered Aug 05, 2020 – Aug 05, 2025Expired

Registration details

Analysis ID: cde2585830f2780b18bfbb58d370ffee
License Form: Ministry of Health Medical Device Manufacturing No. 008488

Company information

Manufacturer: HUA SHENG INSTRUMENTS CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HUA SHENG INSTRUMENTS CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I1800 inspection mirror and accessories
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Aug 05, 2020
Expiry Date: Aug 05, 2025

About this record

Access comprehensive regulatory information for "Huasheng" Speculum and Accessories (Non-Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number cde2585830f2780b18bfbb58d370ffee and manufactured by HUA SHENG INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is HUA SHENG INSTRUMENTS CO., LTD..

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