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"Ostine" steleanalysis software - Taiwan Registration d69bb2fa437b08ee6fe5c6b5a9ae5225

Access comprehensive regulatory information for "Ostine" steleanalysis software in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number d69bb2fa437b08ee6fe5c6b5a9ae5225 and manufactured by OSSTEM IMPLANT Co., Ltd.. The authorized representative in Taiwan is OSSTEM CORPORATION.

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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d69bb2fa437b08ee6fe5c6b5a9ae5225
Registration Details
Taiwan FDA Registration: d69bb2fa437b08ee6fe5c6b5a9ae5225
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Device Details

"Ostine" steleanalysis software
TW: โ€œๆญ่ฉฉๆฑ€โ€ ๆธฌ้กฑๅˆ†ๆž่ปŸ้ซ”
Risk Class 2

Registration Details

d69bb2fa437b08ee6fe5c6b5a9ae5225

DHA05603744301

Company Information

Korea, Republic of

Product Details

Details are as detailed as approved Chinese instructions

P Radiology Science

P.2050 Medical image management and processing systems

import

Dates and Status

Oct 24, 2024

Oct 24, 2029