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"HEIWA" Therapeutic medical binder (Non-Sterile) - Taiwan Registration aba0080320d1751f998861e08ea6a2b4

Access comprehensive regulatory information for "HEIWA" Therapeutic medical binder (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 aba0080320d1751f998861e08ea6a2b4 and manufactured by HEIWA ELECTRONIC INDUSTRIAL CO. LTD. The authorized representative in Taiwan is GOOD LINE INCORPORATION.

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including HEIWA ELECTRONIC INDUSTRIAL CO. LTD, and 1 recent registrations in the same category. 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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aba0080320d1751f998861e08ea6a2b4
Registration Details
Taiwan FDA Registration: aba0080320d1751f998861e08ea6a2b4
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Device Details

"HEIWA" Therapeutic medical binder (Non-Sterile)
TW: "ๅนณๅ’Œ" ้†ซ็™‚็”จๆŸๅธถ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

aba0080320d1751f998861e08ea6a2b4

Ministry of Health Medical Device Import Registration No. 017428

DHA08401742804

Company Information

Product Details

J General hospital and personal use equipment

J5160 Medical straps

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2022

Cancellation Information

Logged out

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