Taiwan FDA registration e031964c3977ab6e8462383fbf42ec90
“Sunoptic” Xenon light source
TW: “桑奧迪”內視鏡用光源裝置
Taiwan·Risk Class 2·MD·SUNOPTIC TECHNOLOGIES, LLC·Registered Aug 26, 2014 – Aug 26, 2019CancelledRegistration details
- Analysis ID
- e031964c3977ab6e8462383fbf42ec90
- License Form
- Ministry of Health Medical Device Import No. 026486
- Customs Code
- DHA05602648608
Company information
- Manufacturer
- SUNOPTIC TECHNOLOGIES, LLC
- Manufacturer Country
- United States
- Authorized Representative
- MATECH HEALTHCARE CORPORATION
Product details
- Product Type (Level 1)
- H Gastroenterology-urology devices
- Product Type (Level 2)
- H1500 endoscope and accessories
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Aug 26, 2014
- Expiry Date
- Aug 26, 2019
- Cancellation Date
- Jul 15, 2022
Cancellation information
- Status
- Logged out
- Reason
- 未展延而逾期者
About this record
Access comprehensive regulatory information for “Sunoptic” Xenon light source in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number e031964c3977ab6e8462383fbf42ec90 and manufactured by SUNOPTIC TECHNOLOGIES, LLC. The authorized representative in Taiwan is MATECH HEALTHCARE CORPORATION.
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