Taiwan FDA registration fae98f54daba308e270191dbe47a44da

"Difu" Aiqiang reconstructive artificial knee system

TW: “帝富”愛強重建型人工膝關節系統
Taiwan flagTaiwan·Risk Class 2·DePuy (Ireland);;DePuy Orthopaedics,Inc.·Registered Jun 28, 2019 – Jun 28, 2029Active
Registration details
Analysis ID
fae98f54daba308e270191dbe47a44da
Customs Code
DHA05603272703
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
Jun 28, 2019
Expiry Date
Jun 28, 2029
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About this record

Access comprehensive regulatory information for "Difu" Aiqiang reconstructive artificial knee system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fae98f54daba308e270191dbe47a44da 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);;DEPUY ORTHOPAEDICS, INC., 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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