Taiwan FDA registration fd0ee8ea1dd78082180bc3fc51d7f3ef

CHUAN SHUN COLD PACK (Non-Sterile)

TW: 銓順冷敷包 (未滅菌)

Taiwan·Risk Class 1·MD·Quanshun Enterprise Co., Ltd. Xinzhuang factory·Registered Oct 01, 2021 – Oct 31, 2023Expired

Registration details

Analysis ID: fd0ee8ea1dd78082180bc3fc51d7f3ef
License Form: Ministry of Health Medical Device Manufacturing Registration No. 002124

Company information

Manufacturer: Quanshun Enterprise Co., Ltd. Xinzhuang factory
Manufacturer Country: Taiwan, Province of China
Authorized Representative: CHUAN SHUN ENTERPRISES CO., LTD.

Product details

Intended Use: Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O5700 Medical Cold Pack
Import Information: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2023

About this record

Access comprehensive regulatory information for CHUAN SHUN COLD PACK (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 fd0ee8ea1dd78082180bc3fc51d7f3ef and manufactured by Quanshun Enterprise Co., Ltd. Xinzhuang factory. The authorized representative in Taiwan is CHUAN SHUN ENTERPRISES 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.