"Integra-Luxtec" fiberoptic light source and carrier (Non-Sterile) - Taiwan Registration ef894d14a6c47fc834299a0a56f58233
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.
Device Details
Registration Details
ef894d14a6c47fc834299a0a56f58233
Ministry of Health Medical Device Import No. 021406
DHA09402140605
Product Details
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)".
G ENT device
G4350 ENT fiber optic light source and vehicle
Imported from abroad
Dates and Status
Mar 26, 2020
Mar 26, 2025