Taiwan FDA registration 43b99442ab8ae614332662f6447a2e16
"SyncVision" Speculum and Accessories (Non-Sterile)
TW: "杏澤" 檢查鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·SYNCVISION TECHNOLOGY CORPORATION·Registered Aug 26, 2020 – Aug 26, 2025ExpiredRegistration details
- Analysis ID
- 43b99442ab8ae614332662f6447a2e16
- License Form
- Ministry of Health Medical Device Manufacturing No. 008556
Company information
- Manufacturer
- SYNCVISION TECHNOLOGY CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- SYNCVISION TECHNOLOGY CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Devices "Examination Scopes and Their Accessories (I.1800)".
- Product Type (Level 1)
- I General and plastic surgical devices
- Product Type (Level 2)
- I1800 inspection mirror and accessories
- Import Information
- Produced in Taiwan, China
Dates and status
- Registration Date
- Aug 26, 2020
- Expiry Date
- Aug 26, 2025
About this record
Access comprehensive regulatory information for "SyncVision" Speculum and Accessories (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 43b99442ab8ae614332662f6447a2e16 and manufactured by SYNCVISION TECHNOLOGY CORPORATION. The authorized representative in Taiwan is SYNCVISION TECHNOLOGY CORPORATION.
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