Taiwan FDA registration ca8dfc252a25c8890e6a8af946ebbe92

"Bunme" Stanac sternum fixation system

TW: “邦美”史塔納克胸骨固定系統
Taiwan flagTaiwan·Risk Class 2·BIOMET MICROFIXATION ;; BIOMET INC.·Registered Sep 21, 2022 – Sep 21, 2027Active
Registration details
Analysis ID
ca8dfc252a25c8890e6a8af946ebbe92
Customs Code
DHA05603590707
Company information
Manufacturer Country
United States
Authorized Representative
ZIMMER BIOMET TAIWAN CO., LTD.
Product details
Intended Use
Details are as detailed as approved Chinese instructions
Product Type (Level 1)
N Orthopedics
Product Type (Level 2)
N.3030 Single or multiple metallic bone fixation devices and accessories
Import Information
Input;; Contract manufacturing
Dates and status
Registration Date
Sep 21, 2022
Expiry Date
Sep 21, 2027
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About this record

Access comprehensive regulatory information for "Bunme" Stanac sternum fixation system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number ca8dfc252a25c8890e6a8af946ebbe92 and manufactured by BIOMET MICROFIXATION ;; BIOMET INC.. 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 Microfixation;; Changzhou Biomet Medical Devices Co., 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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