Taiwan FDA registration 38df0753d6bd60cbdd4c5773785d51c4

"Biotroin" Oropharyngeal Airway (Non-Sterile)

TW: "亞仕丹'口咽氣道管(未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·THE LARYNGEAL MASK COMPANY LIMITED·Registered Sep 17, 2015 – Sep 17, 2020Cancelled
Registration details
Analysis ID
38df0753d6bd60cbdd4c5773785d51c4
License Form
Ministry of Health Medical Device Import No. 015684
Customs Code
DHA09401568408
Company information
Manufacturer Country
United States
Authorized Representative
BIOTRONIC INSTRUMENT ENTERPRISE LTD.
Product details
Product Type (Level 1)
D Devices for anesthesiology
Product Type (Level 2)
D5110 Oropharyngeal airway tube
Import Information
Imported from abroad
Dates and status
Registration Date
Sep 17, 2015
Expiry Date
Sep 17, 2020
Cancellation Date
Jul 15, 2022
Cancellation information
Status
Logged out
Reason
未展延而逾期者
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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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