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“OsseoFuse” Frequency Analyzer (non-sterile) - Taiwan Registration 58b71def1ca1c3f6e8eafb13c8716a36

Access comprehensive regulatory information for “OsseoFuse” Frequency Analyzer (non-sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 58b71def1ca1c3f6e8eafb13c8716a36 and manufactured by OSSEOFUSE INTERNATIONAL INC.. The authorized representative in Taiwan is LEGREEN PROPERTIES LIMITED, TAIWAN BRANCH BVI.

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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58b71def1ca1c3f6e8eafb13c8716a36
Registration Details
Taiwan FDA Registration: 58b71def1ca1c3f6e8eafb13c8716a36
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Device Details

“OsseoFuse” Frequency Analyzer (non-sterile)
TW: “艾秀菲絲” 牙科植體穩定分析儀 (未滅菌)
Risk Class 1
MD

Registration Details

58b71def1ca1c3f6e8eafb13c8716a36

Ministry of Health Medical Device Import No. 022365

DHA09402236509

Company Information

United States

Product Details

Limited to the first level recognition range of medical equipment management measures dental handpieces and their accessories (F.4200).

F Dental devices

F4200 Dental Handpiece and its accessories

Imported from abroad

Dates and Status

Mar 08, 2021

Mar 08, 2026