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"Guofa" restraint belt (unsterilized) - Taiwan Registration 4f76b020ce2fe545c82484df5f8c3b46

Access comprehensive regulatory information for "Guofa" restraint belt (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 4f76b020ce2fe545c82484df5f8c3b46 and manufactured by K.F. MEDICAL INSTRUMENTS CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including K.F. MEDICAL INSTRUMENTS 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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4f76b020ce2fe545c82484df5f8c3b46
Registration Details
Taiwan FDA Registration: 4f76b020ce2fe545c82484df5f8c3b46
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Device Details

"Guofa" restraint belt (unsterilized)
TW: "ๅœ‹็™ผ" ็ด„ๆŸๅธถ(ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

4f76b020ce2fe545c82484df5f8c3b46

DHY04300043600

Company Information

Taiwan, Province of China

Product Details

For the purpose of restricting the movement of the patient during treatment or examination and to protect the patient or others due to medical necessity.

J General hospital and personal use equipment

J.6760 ไฟ่ญทๆ€ง้™ๅˆถๅธถ

Domestic

Dates and Status

Oct 20, 2005

Oct 20, 2015

Apr 25, 2018

Cancellation Information

Logged out

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