Taiwan FDA registration e9b6bfaf16fe787e8147c80c63249de2
"DermLite" Speculum and accessories (Non-Sterile)
TW: "德萊特" 檢查鏡及其附件 (未滅菌)
Taiwan·Risk Class 1·MD·DermLite, LLC·Registered Nov 04, 2020 – Nov 04, 2025ExpiredRegistration details
- Analysis ID
- e9b6bfaf16fe787e8147c80c63249de2
- License Form
- Ministry of Health Medical Device Import No. 022082
- Customs Code
- DHA09402208200
Company information
- Manufacturer
- DermLite, LLC
- Manufacturer Country
- United States
- Authorized Representative
- GOLDENSPRING MEDI-TECH CO., LTD.
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
- Imported from abroad
Dates and status
- Registration Date
- Nov 04, 2020
- Expiry Date
- Nov 04, 2025
About this record
Access comprehensive regulatory information for "DermLite" 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 e9b6bfaf16fe787e8147c80c63249de2 and manufactured by DermLite, LLC. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..
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