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“Zimmer Biomet Spine” Timberline MPF System - Taiwan Registration 609d7c29006c40f6ec556045845ae1aa

Access comprehensive regulatory information for “Zimmer Biomet Spine” Timberline MPF System in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 609d7c29006c40f6ec556045845ae1aa and manufactured by ZIMMER BIOMET SPINE, INC.. The authorized representative in Taiwan is ZimVie 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.

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609d7c29006c40f6ec556045845ae1aa
Registration Details
Taiwan FDA Registration: 609d7c29006c40f6ec556045845ae1aa
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Device Details

“Zimmer Biomet Spine” Timberline MPF System
TW: “捷邁”帝博萊脊椎融合系統
Risk Class 2
MD

Registration Details

609d7c29006c40f6ec556045845ae1aa

Ministry of Health Medical Device Import No. 033647

DHA05603364700

Company Information

United States

Product Details

For details, it is Chinese approved copy of the imitation order

N Orthopedic devices

N3080 Interbody fusion device

Imported from abroad

Dates and Status

May 16, 2020

May 16, 2025