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OPPO Cold/Hot Pack (Non-sterile) - Taiwan Registration b38c0d8f326feff1a5a4639e8fd81ee9

Access comprehensive regulatory information for OPPO 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 b38c0d8f326feff1a5a4639e8fd81ee9 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.

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b38c0d8f326feff1a5a4639e8fd81ee9
Registration Details
Taiwan FDA Registration: b38c0d8f326feff1a5a4639e8fd81ee9
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Device Details

OPPO Cold/Hot Pack (Non-sterile)
TW: OPPOๅ†ท็†ฑๆ•ทๅŒ… (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

b38c0d8f326feff1a5a4639e8fd81ee9

Ministry of Health Medical Device Manufacturing Registration No. 004940

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