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“PROXER”Cold/Hot pack (Non-sterile) - Taiwan Registration 927c1849e1a076478e07626f0962ebfc

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.

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927c1849e1a076478e07626f0962ebfc
Registration Details
Taiwan FDA Registration: 927c1849e1a076478e07626f0962ebfc
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Device Details

“PROXER”Cold/Hot pack (Non-sterile)
TW: “博瑟” 冷熱敷墊(未滅菌)
Risk Class 1
MD

Registration Details

927c1849e1a076478e07626f0962ebfc

Ministry of Health Medical Device Manufacturing Registration No. 005038

Company Information

Taiwan, Province of China

Product Details

Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Medical Cold Compress Pack (O.5700)".

o Equipment for physical medicine

O5700 Medical Cold Pack

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2024