Taiwan FDA registration 4647a50e1ea846a21adac520c572b284

LP Cold/Hot Pack (Non-sterile)

TW: LP冷熱敷包 (未滅菌)

Taiwan·Risk Class 1·MD·PLUS MEDITECH CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2024Expired

Registration details

Analysis ID: 4647a50e1ea846a21adac520c572b284
License Form: Ministry of Health Medical Device Manufacturing Registration No. 004949

Company information

Manufacturer: PLUS MEDITECH CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: PLUS MEDITECH 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, 2024

About this record

Access comprehensive regulatory information for LP Cold/Hot 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 4647a50e1ea846a21adac520c572b284 and manufactured by PLUS MEDITECH CO., LTD.. The authorized representative in Taiwan is PLUS MEDITECH 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.