Taiwan FDA registration ffa9dff2b89571dd8f3999fada2b0388
ISOLUX LIGHT SOURCE AND ACCESSORIES (Non-Sterile)
TW: 愛索羅斯光源及附件 (未滅菌)
Taiwan·Risk Class 1·MD·ISOLUX LLC·Registered Mar 16, 2021 – Mar 16, 2026ExpiredRegistration details
- Analysis ID
- ffa9dff2b89571dd8f3999fada2b0388
- License Form
- Ministry of Health Medical Device Import No. 022388
- Customs Code
- DHA09402238808
Company information
- Manufacturer
- ISOLUX LLC
- Manufacturer Country
- United States
- Authorized Representative
- BOSHIN LIGHTING COMPANY LIMITED
Product details
- Intended Use
- Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Fiber Optic Light Source and Vehicle (G.4350)".
- Product Type (Level 1)
- G ENT device
- Product Type (Level 2)
- G4350 ENT fiber optic light source and vehicle
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 16, 2021
- Expiry Date
- Mar 16, 2026
About this record
Access comprehensive regulatory information for ISOLUX LIGHT SOURCE 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 ffa9dff2b89571dd8f3999fada2b0388 and manufactured by ISOLUX LLC. The authorized representative in Taiwan is BOSHIN LIGHTING COMPANY LIMITED.
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