Taiwan FDA registration 927c1849e1a076478e07626f0962ebfc

“PROXER”Cold/Hot pack (Non-sterile)

TW: “博瑟” 冷熱敷墊(未滅菌)

Taiwan·Risk Class 1·MD·R&R MEDICAL CORPORATION LTD.·Registered Oct 01, 2021 – Oct 31, 2024Expired

Registration details

Analysis ID: 927c1849e1a076478e07626f0962ebfc
License Form: Ministry of Health Medical Device Manufacturing Registration No. 005038

Company information

Manufacturer: R&R MEDICAL CORPORATION LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: R&R MEDICAL CORPORATION 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 “PROXER”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 927c1849e1a076478e07626f0962ebfc and manufactured by R&R MEDICAL CORPORATION LTD.. The authorized representative in Taiwan is R&R MEDICAL CORPORATION 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.