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Oshifi implant system - Taiwan Registration e98e5be004627b3fc0a9b8603bc44c12

Access comprehensive regulatory information for Oshifi implant system in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 3 medical device is registered under number e98e5be004627b3fc0a9b8603bc44c12 and manufactured by ANTHOGYR SAS. The authorized representative in Taiwan is TSENG LIMITED.

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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e98e5be004627b3fc0a9b8603bc44c12
Registration Details
Taiwan FDA Registration: e98e5be004627b3fc0a9b8603bc44c12
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Device Details

Oshifi implant system
TW: ๆญไป•่ฒๆค้ซ”็ณป็ตฑ
Risk Class 3
Cancelled

Registration Details

e98e5be004627b3fc0a9b8603bc44c12

DHA00601978903

Company Information

France

Product Details

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

F Dentistry

F.3640 Bone Implants

import

Dates and Status

Apr 20, 2009

Apr 20, 2019

Nov 22, 2022

Cancellation Information

Logged out

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