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"K.F." Splint(Non-Sterile) - Taiwan Registration 15737c505b396eb57f09fa3d27bfc7c9

Access comprehensive regulatory information for "K.F." Splint(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 15737c505b396eb57f09fa3d27bfc7c9 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. 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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15737c505b396eb57f09fa3d27bfc7c9
Registration Details
Taiwan FDA Registration: 15737c505b396eb57f09fa3d27bfc7c9
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Device Details

"K.F." Splint(Non-Sterile)
TW: "ๅœ‹็™ผ"ๅ›บๅฎšๅธถ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

15737c505b396eb57f09fa3d27bfc7c9

Ministry of Health Medical Device Manufacturing Registration No. 000482

DHY08300048204

Company Information

Taiwan, Province of China

Product Details

It is used to support or immobilize fractures, injuries with excessive force or sprains to the trunk.

o Equipment for physical medicine

O3490 Torso Gear

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025