Taiwan FDA registration d69bb2fa437b08ee6fe5c6b5a9ae5225
"Ostine" steleanalysis software
TW: “歐詩汀” 測顱分析軟體
Taiwan·Risk Class 2·OSSTEM IMPLANT Co., Ltd.·Registered Oct 24, 2024 – Oct 24, 2029ActiveRegistration details
- Analysis ID
- d69bb2fa437b08ee6fe5c6b5a9ae5225
- Customs Code
- DHA05603744301
Company information
- Manufacturer
- OSSTEM IMPLANT Co., Ltd.
- Manufacturer Country
- Korea, Republic of
- Authorized Representative
- OSSTEM CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- P Radiology Science
- Product Type (Level 2)
- P.2050 Medical image management and processing systems
- Import Information
- import
Dates and status
- Registration Date
- Oct 24, 2024
- Expiry Date
- Oct 24, 2029
About this record
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.
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