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"Difu" Ressis artificial knee joint - Taiwan Registration 59100d40b6d2cf51348dae01f2b0ffb7

Access comprehensive regulatory information for "Difu" Ressis artificial knee joint in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 59100d40b6d2cf51348dae01f2b0ffb7 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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59100d40b6d2cf51348dae01f2b0ffb7
Registration Details
Taiwan FDA Registration: 59100d40b6d2cf51348dae01f2b0ffb7
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Device Details

"Difu" Ressis artificial knee joint
TW: "ๅธๅฏŒ" ้›ท่ฅฟๅฃซไบบๅทฅ่†้—œ็ฏ€
Risk Class 2
Cancelled

Registration Details

59100d40b6d2cf51348dae01f2b0ffb7

DHA00600955702

Company Information

United States

Product Details

N000 Orthopedics

import

Dates and Status

Nov 16, 2000

Nov 16, 2015

Apr 25, 2018

Cancellation Information

Logged out

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