"Integra-Luxtec" fiberoptic light source and carrier (Non-Sterile)
Taiwan·Risk Class 1·MD·Integra Burlington MA, Inc.·Registered Mar 26, 2020 – Mar 26, 2025Expired- Analysis ID
- ef894d14a6c47fc834299a0a56f58233
- License Form
- Ministry of Health Medical Device Import No. 021406
- Customs Code
- DHA09402140605
- Manufacturer
- Integra Burlington MA, Inc.
- Manufacturer Country
- United States
- Authorized Representative
- ASIA-COL INTERNATIONAL CO., LTD.
- 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
- Registration Date
- Mar 26, 2020
- Expiry Date
- Mar 26, 2025
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Access comprehensive regulatory information for "Integra-Luxtec" fiberoptic light source and carrier (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 ef894d14a6c47fc834299a0a56f58233 and manufactured by Integra Burlington MA, Inc.. The authorized representative in Taiwan is ASIA-COL INTERNATIONAL CO., LTD..
This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including Integra LifeSciences (Ireland) Ltd., and 1 recent registrations in the same category. Pure Global AI offers free access to 89,000+ Taiwan medical device registrations, helping global MedTech companies navigate Taiwan FDA regulations, identify competitors, and discover partnership opportunities efficiently.