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"Integra" Ear, nose, and throat manual surgical instrument (Sterile) - Taiwan Registration 77088826e4667711ceabdeff0cd16d1e

Access comprehensive regulatory information for "Integra" Ear, nose, and throat manual surgical instrument (Sterile) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 77088826e4667711ceabdeff0cd16d1e and manufactured by INTEGRA YORK PA, INC.. The authorized representative in Taiwan is ANGEL MEDICAL INSTRUMENT 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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77088826e4667711ceabdeff0cd16d1e
Registration Details
Taiwan FDA Registration: 77088826e4667711ceabdeff0cd16d1e
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Device Details

"Integra" Ear, nose, and throat manual surgical instrument (Sterile)
TW: "่‹ฑ็‰นๆ ผ็ˆพ" ่€ณ้ผปๅ–‰ๆ‰‹ๅ‹•ๅผๅค–็ง‘ๅ™จๆขฐ (ๆป…่Œ)
Risk Class 1
MD

Registration Details

77088826e4667711ceabdeff0cd16d1e

Ministry of Health Medical Device Import No. 017095

DHA09401709502

Company Information

United States

Product Details

Limited to the first level identification scope of the Measures for the Administration of Medical Devices "ENT Manual Surgical Instruments (G.4420)".

G ENT device

G4420 OTOLARYNGARY Manual Surgical Instrument

Imported from abroad; GMP

Dates and Status

Oct 18, 2016

Oct 18, 2026