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"Biotroin" Oropharyngeal Airway (Non-Sterile) - Taiwan Registration 38df0753d6bd60cbdd4c5773785d51c4

Access comprehensive regulatory information for "Biotroin" Oropharyngeal 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 38df0753d6bd60cbdd4c5773785d51c4 and manufactured by THE LARYNGEAL MASK COMPANY LIMITED. The authorized representative in Taiwan is BIOTRONIC INSTRUMENT ENTERPRISE LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including THE LARYNGEAL MASK COMPANY LIMITED, 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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38df0753d6bd60cbdd4c5773785d51c4
Registration Details
Taiwan FDA Registration: 38df0753d6bd60cbdd4c5773785d51c4
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Device Details

"Biotroin" Oropharyngeal Airway (Non-Sterile)
TW: "ไบžไป•ไธน'ๅฃๅ’ฝๆฐฃ้“็ฎก(ๆœชๆป…่Œ)
Risk Class 1
MD
Cancelled

Registration Details

38df0753d6bd60cbdd4c5773785d51c4

Ministry of Health Medical Device Import No. 015684

DHA09401568408

Company Information

United States

Product Details

D Devices for anesthesiology

D5110 Oropharyngeal airway tube

Imported from abroad

Dates and Status

Sep 17, 2015

Sep 17, 2020

Jul 15, 2022

Cancellation Information

Logged out

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