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"K.F." FINGER SPLINT(NON-STERILE) - Taiwan Registration e7b9dde85a2d0a1ee37cb05ec1b994a0

Access comprehensive regulatory information for "K.F." FINGER 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 e7b9dde85a2d0a1ee37cb05ec1b994a0 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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e7b9dde85a2d0a1ee37cb05ec1b994a0
Registration Details
Taiwan FDA Registration: e7b9dde85a2d0a1ee37cb05ec1b994a0
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Device Details

"K.F." FINGER SPLINT(NON-STERILE)
TW: "ๅœ‹็™ผ" ๆ‰‹ๆŒ‡่ญทๆœจ(ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

e7b9dde85a2d0a1ee37cb05ec1b994a0

Ministry of Health Medical Device Manufacturing Registration No. 000025

DHY08300002502

Company Information

Taiwan, Province of China

Product Details

Used to support, correct or prevent deformation.

o Equipment for physical medicine

O3475 Body Equipment

Produced in Taiwan, China

Dates and Status

Oct 01, 2021

Oct 31, 2025