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"Intergra" Ear, nose, and throat fiberoptic light source and carrier (Non-sterile) - Taiwan Registration 466238f240d9308f471b76e8c4db0ad7

Access comprehensive regulatory information for "Intergra" Ear, nose, and throat 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 466238f240d9308f471b76e8c4db0ad7 and manufactured by INTERGRA YORK PA, INC. The authorized representative in Taiwan is TRANSMEDIC CO., LTD..

This page provides complete technical specifications, regulatory compliance details. 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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466238f240d9308f471b76e8c4db0ad7
Registration Details
Taiwan FDA Registration: 466238f240d9308f471b76e8c4db0ad7
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Device Details

"Intergra" Ear, nose, and throat fiberoptic light source and carrier (Non-sterile)
TW: "่‹ฑ็‰นๆ ผๆ‹‰" ่€ณ้ผปๅ–‰ๅ…‰็บ–ๅ…‰ๆบๅŠ่ผ‰ๅ…ท (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

466238f240d9308f471b76e8c4db0ad7

Ministry of Health Medical Device Import No. 015602

DHA09401560206

Company Information

United States

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

Aug 25, 2015

Aug 25, 2025