Taiwan FDA registration 2e9e90ae67343351f8e3b62d1ee5b844

“Biomet” Vanguard Knee System

TW: “邦美”先鋒人工膝關節系統
Taiwan flagTaiwan·Risk Class 2·MD·BIOMET ORTHOPEDICS·Registered Apr 26, 2017 – Apr 26, 2022Expired
Registration details
Analysis ID
2e9e90ae67343351f8e3b62d1ee5b844
License Form
Ministry of Health Medical Device Import No. 029650
Customs Code
DHA05602965000
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)
N3560 Semi-restrictive knee femoral tibial polymer/metal/polymeric cement compound
Import Information
Imported from abroad
Dates and status
Registration Date
Apr 26, 2017
Expiry Date
Apr 26, 2022
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About this record

Access comprehensive regulatory information for “Biomet” Vanguard 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 2e9e90ae67343351f8e3b62d1ee5b844 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, 1 companies making similar products including BIOMET ORTHOPEDICS, 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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