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“NuVasive” AttraX Scaffold - Taiwan Registration 0724c2f59de0535481ccd41b4312e955

Access comprehensive regulatory information for “NuVasive” AttraX Scaffold in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 0724c2f59de0535481ccd41b4312e955 and manufactured by NuVasive Inc.. The authorized representative in Taiwan is MAXIGEN BIOTECH INC..

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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0724c2f59de0535481ccd41b4312e955
Registration Details
Taiwan FDA Registration: 0724c2f59de0535481ccd41b4312e955
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Device Details

“NuVasive” AttraX Scaffold
TW: “紐瓦索”艾特骨骼填補物
Risk Class 2
MD

Registration Details

0724c2f59de0535481ccd41b4312e955

Ministry of Health Medical Device Import No. 034962

DHA05603496200

Company Information

United States

Product Details

Details are as detailed as approved Chinese instructions

N Orthopedic devices

N3045 Absorbable calcium salt bone cavity filling device

Imported from abroad

Dates and Status

Sep 28, 2021

Sep 28, 2026