Taiwan FDA registration 69f9e42a2bda11b6b8b35d959c11f27e

"Difu" knee gama femur assembly

TW: “帝富”膝格瑪股骨組件
Taiwan flagTaiwan·Risk Class 2·DePuy (Ireland);;DEPUY ORTHOPAEDICS, INC.·Registered May 16, 2011 – May 16, 2026Expired
Registration details
Analysis ID
69f9e42a2bda11b6b8b35d959c11f27e
Customs Code
DHA00602239607
Company information
Manufacturer Country
Ireland;;United States
Authorized Representative
JOHNSON & JOHNSON MEDICAL TAIWAN LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3560 Semi-restrictive knee joints of the femoral bone polymers/metallics/polymers
Import Information
import
Dates and status
Registration Date
May 16, 2011
Expiry Date
May 16, 2026
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About this record

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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