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"Integra-Luxtec" fiberoptic light source and carrier (non-sterile) - Taiwan Registration f936437ab028bc6e514ea4627be1d2ae

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.

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f936437ab028bc6e514ea4627be1d2ae
Registration Details
Taiwan FDA Registration: f936437ab028bc6e514ea4627be1d2ae
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Device Details

"Integra-Luxtec" fiberoptic light source and carrier (non-sterile)
TW: "่‹ฑ็‰นๆˆˆๆ‹‰-ๆ‹‰็‰นๆ–ฏ" ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

f936437ab028bc6e514ea4627be1d2ae

Ministry of Health Medical Device Import No. 022028

DHA09402202804

Company Information

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

Oct 14, 2020

Oct 14, 2025

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