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"Difu" knee gama femur assembly - Taiwan Registration 69f9e42a2bda11b6b8b35d959c11f27e

Access comprehensive regulatory information for "Difu" knee gama femur assembly in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 69f9e42a2bda11b6b8b35d959c11f27e and manufactured by DePuy (Ireland);;DEPUY ORTHOPAEDICS, INC.. The authorized representative in Taiwan is JOHNSON & JOHNSON MEDICAL TAIWAN LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including DEPUY (IRELAND) LIMITED;; DEPUY INTERNATIONAL LTD., and 1 recent registrations in the same category. 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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69f9e42a2bda11b6b8b35d959c11f27e
Registration Details
Taiwan FDA Registration: 69f9e42a2bda11b6b8b35d959c11f27e
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Device Details

"Difu" knee gama femur assembly
TW: โ€œๅธๅฏŒโ€่†ๆ ผ็‘ช่‚ก้ชจ็ต„ไปถ
Risk Class 2

Registration Details

69f9e42a2bda11b6b8b35d959c11f27e

DHA00602239607

Company Information

Ireland;;United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedics

N.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers

import

Dates and Status

May 16, 2011

May 16, 2026

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