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"I-M" HERNIA SUPPORT (Non-Sterile) - Taiwan Registration 836012a4eba2663d4f9134c04345400d

Access comprehensive regulatory information for "I-M" 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 836012a4eba2663d4f9134c04345400d and manufactured by Aimin Eisai Co., Ltd. Plant 2. The authorized representative in Taiwan is Aimin Eisai Co., Ltd. Plant 2.

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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836012a4eba2663d4f9134c04345400d
Registration Details
Taiwan FDA Registration: 836012a4eba2663d4f9134c04345400d
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Device Details

"I-M" HERNIA SUPPORT (Non-Sterile)
TW: "ๆ„›ๆฐ‘" ็–่„ซๆ”ฏๆ’ๅ™จ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

836012a4eba2663d4f9134c04345400d

Ministry of Health Medical Device Manufacturing Registration No. 000089

DHY08300008902

Company Information

Taiwan, Province of China

Product Details

H Gastroenterology-urology devices

H5970 Hernia Brace

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025

Oct 28, 2022

Cancellation Information

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