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"Difu" knee gama femur assembly - Taiwan Registration 1f2b6b3fcf9145c12567ad4c773b614b

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 1f2b6b3fcf9145c12567ad4c773b614b and manufactured by DEPUY (IRELAND) LIMITED;; DEPUY INTERNATIONAL LTD.. 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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1f2b6b3fcf9145c12567ad4c773b614b
Registration Details
Taiwan FDA Registration: 1f2b6b3fcf9145c12567ad4c773b614b
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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

1f2b6b3fcf9145c12567ad4c773b614b

DHA05602696405

Company Information

Ireland;;United Kingdom

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

Jan 23, 2015

Jan 23, 2025

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