Taiwan FDA registration 6ed8d0ce9fe325eacdc806ca0e52c389

"Jetway" light nose organ

TW: “捷威”光鼻器
Taiwan flagTaiwan·Risk Class 2·MESURE TECHNOLOGY CO., LTD.·Registered Jul 15, 2008 – Jul 15, 2023Expired
Registration details
Analysis ID
6ed8d0ce9fe325eacdc806ca0e52c389
Customs Code
DHY00500248006
Company information
Manufacturer Country
Taiwan, Province of China
Authorized Representative
MESURE TECHNOLOGY CO., LTD.
Product details
Intended Use
Helps relieve symptoms such as nasal congestion, runny nose, sneezing caused by allergic rhinitis, and should not be used by children under 12 years of age.
Product Type (Level 1)
I General, Plastic Surgery and Dermatology
Product Type (Level 2)
I.4810 Lasers for general surgical, orthopaedic and dermatological use
Import Information
Domestic
Dates and status
Registration Date
Jul 15, 2008
Expiry Date
Jul 15, 2023
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About this record

Access comprehensive regulatory information for "Jetway" light nose organ in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number 6ed8d0ce9fe325eacdc806ca0e52c389 and manufactured by MESURE TECHNOLOGY CO., LTD.. The authorized representative in Taiwan is MESURE TECHNOLOGY CO., LTD..

This page provides complete technical specifications, regulatory compliance details, 1 companies making similar products including MESURE TECHNOLOGY CO., LTD., and 2 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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