Taiwan FDA registration 401c2e6c8424122454b17dcc99d266f0

“Biomet” Hip Joint Replacement Prostheses Echo Femoral Stem

TW: “邦美”人工髖關節艾可股骨柄
Taiwan flagTaiwan·Risk Class 2·MD·BIOMET ORTHOPEDICS·Registered Nov 07, 2017 – Nov 07, 2022Expired
Registration details
Analysis ID
401c2e6c8424122454b17dcc99d266f0
License Form
Ministry of Health Medical Device Import No. 030380
Customs Code
DHA05603038007
Company information
Manufacturer
BIOMET ORTHOPEDICS
Manufacturer Country
United States
Authorized Representative
ZIMMER BIOMET TAIWAN CO., LTD.
Product details
Intended Use
For details, it is Chinese approved copy of the imitation order
Product Type (Level 1)
N Orthopedic devices
Product Type (Level 2)
N3330 Semi-restricted hip metal/metal containing non-cement acetabular components
Import Information
Imported from abroad
Dates and status
Registration Date
Nov 07, 2017
Expiry Date
Nov 07, 2022
About this record

Access comprehensive regulatory information for “Biomet” Hip Joint Replacement Prostheses Echo Femoral Stem in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 401c2e6c8424122454b17dcc99d266f0 and manufactured by BIOMET ORTHOPEDICS. The authorized representative in Taiwan is ZIMMER BIOMET TAIWAN CO., 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.

Free DatabasePowered by Pure Global AI89,000+ Devices