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"Guofa Jintan" restraint belt (unsterilized) - Taiwan Registration 8afc4b05523f943afd619f640f39be0d

Access comprehensive regulatory information for "Guofa Jintan" 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 8afc4b05523f943afd619f640f39be0d and manufactured by YEH SHINE (JIN TAN) MEDICAL SUPPLIES CO., LTD.. The authorized representative in Taiwan is K.F. MEDICAL INSTRUMENTS 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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8afc4b05523f943afd619f640f39be0d
Registration Details
Taiwan FDA Registration: 8afc4b05523f943afd619f640f39be0d
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Device Details

"Guofa Jintan" restraint belt (unsterilized)
TW: โ€œๅœ‹็™ผ้‡‘ๅฃ‡โ€็ด„ๆŸๅธถ (ๆœชๆป…่Œ)
Risk Class 1
Cancelled

Registration Details

8afc4b05523f943afd619f640f39be0d

DHA04600055005

Company Information

Product Details

It is limited to the first level of identification scope of the "Protective Restriction Strip (J.6760)" of the Administrative Measures for Medical Devices.

J General hospital and personal use equipment

J.6760 ไฟ่ญทๆ€ง้™ๅˆถๅธถ

Chinese goods;; input

Dates and Status

Jul 30, 2008

Jul 30, 2018

Jun 17, 2022

Cancellation Information

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