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"I-Gel" LARYNGEAL MASK AIRWAY (Non-Sterile) - Taiwan Registration ecc15adcf17c400a5b4002fab295c4a7

Access comprehensive regulatory information for "I-Gel" LARYNGEAL MASK AIRWAY (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 ecc15adcf17c400a5b4002fab295c4a7 and manufactured by INTERSURGICAL LTD.. The authorized representative in Taiwan is FU SHING MEDICAL 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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Registration Details
Taiwan FDA Registration: ecc15adcf17c400a5b4002fab295c4a7
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Device Details

"I-Gel" LARYNGEAL MASK AIRWAY (Non-Sterile)
TW: "่‰พๆท" ๅ–‰้ ญ้ข็ฝฉ (ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

ecc15adcf17c400a5b4002fab295c4a7

Ministry of Health Medical Device Import No. 018085

DHA09401808501

Company Information

Lithuania

Product Details

D Devices for anesthesiology

D5110 Oropharyngeal airway tube

Imported from abroad

Dates and Status

Jul 19, 2017

Jul 19, 2022

Dec 24, 2020

Cancellation Information

Logged out

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