Pure Global

"KLARITY" SPLINT (Non-Sterile) - Taiwan Registration 13dfd6a6b54016bf1a2834e5229011a6

Access comprehensive regulatory information for "KLARITY" 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 13dfd6a6b54016bf1a2834e5229011a6 and manufactured by KLARITY MEDICAL PRODUCTS. The authorized representative in Taiwan is JET INTERNATIONAL MEDICAL 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.

Free Database
Powered by Pure Global AI
89,000+ Devices
13dfd6a6b54016bf1a2834e5229011a6
Registration Details
Taiwan FDA Registration: 13dfd6a6b54016bf1a2834e5229011a6
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing

Device Details

"KLARITY" SPLINT (Non-Sterile)
TW: "็ง‘่Š็‘ž่ฟช" ๅก‘ๆๅคพๆฟ(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

13dfd6a6b54016bf1a2834e5229011a6

Ministry of Health Medical Device Import Registration No. 011907

DHA08401190702

Company Information

United States

Product Details

I General and plastic surgical devices

I3910 Splints for non-inflated extremities

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2022

Cancellation Information

Logged out

ๆœชๅฑ•ๅปถ่€Œ้€พๆœŸ่€