"Integra-Luxtec" fiberoptic light source and carrier (non-sterile)
Taiwan·Risk Class 1·MD·Integra LifeSciences (Ireland) Ltd.·Registered Oct 14, 2020 – Oct 14, 2025Expired- Analysis ID
- f936437ab028bc6e514ea4627be1d2ae
- License Form
- Ministry of Health Medical Device Import No. 022028
- Customs Code
- DHA09402202804
- Manufacturer
- Integra LifeSciences (Ireland) Ltd.
- Manufacturer Country
- Ireland
- 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
- Oct 14, 2020
- Expiry Date
- Oct 14, 2025
Top companies providing products similar to ""Integra-Luxtec" fiberoptic light source and carrier (non-sterile)"
Recently registered similar products
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 f936437ab028bc6e514ea4627be1d2ae and manufactured by Integra LifeSciences (Ireland) Ltd.. 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 Burlington MA, Inc., 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.