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OPPO Hernia Support (Non-sterile) - Taiwan Registration 1d42b534c794d5d2f79a354a9251845b

Access comprehensive regulatory information for OPPO Hernia Support (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 1d42b534c794d5d2f79a354a9251845b 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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1d42b534c794d5d2f79a354a9251845b
Registration Details
Taiwan FDA Registration: 1d42b534c794d5d2f79a354a9251845b
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Device Details

OPPO Hernia Support (Non-sterile)
TW: OPPO็–่„ซๆ”ฏๆ’ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

1d42b534c794d5d2f79a354a9251845b

Ministry of Health Medical Device Manufacturing Registration No. 004933

Company Information

Taiwan, Province of China

Product Details

Limited to the first level recognition range of the hernia brace (H.5970) of the Measures for the Administration of Medical Devices.

H Gastroenterology-urology devices

H5970 Hernia Brace

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2024