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"Difu" Solusi system - Taiwan Registration 84289fd08d3b7169dcf016aa482e81ba

Access comprehensive regulatory information for "Difu" Solusi system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 84289fd08d3b7169dcf016aa482e81ba and manufactured by DEPUY ORTHOPAEDICS,INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN 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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84289fd08d3b7169dcf016aa482e81ba
Registration Details
Taiwan FDA Registration: 84289fd08d3b7169dcf016aa482e81ba
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Device Details

"Difu" Solusi system
TW: "ๅธๅฏŒ" ็ดข้œฒ่ฅฟ็ณป็ตฑ
Risk Class 2
Cancelled

Registration Details

84289fd08d3b7169dcf016aa482e81ba

DHA00600929307

Company Information

United States

Product Details

0399 Other artificial function substitutes

import

Dates and Status

Sep 02, 1999

Sep 14, 2023

Sep 23, 2021

Cancellation Information

Logged out

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