Taiwan FDA registration d41090c2ab688188f7d82fd37bf79b67

“Hong Shiang”eplilator (Non-Sterile)

TW: “鴻祥”除毛機(未滅菌)

Taiwan·Risk Class 1·MD·HONG SHIANG TECHNOLOGY CO., LTD.·Registered Apr 23, 2021 – Apr 23, 2026Expired

Registration details

Analysis ID: d41090c2ab688188f7d82fd37bf79b67
License Form: Ministry of Health Medical Device Manufacturing No. 009051

Company information

Manufacturer: HONG SHIANG TECHNOLOGY CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HONG SHIANG TECHNOLOGY CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Probe Hair Removal Machine (I.5350)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I5350 Probe Hair Remover
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Apr 23, 2021
Expiry Date: Apr 23, 2026

About this record

Access comprehensive regulatory information for “Hong Shiang”eplilator (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 d41090c2ab688188f7d82fd37bf79b67 and manufactured by HONG SHIANG TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is HONG SHIANG TECHNOLOGY CO., LTD..

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