Taiwan FDA registration 609eca6f3abd5011e2488a06d9fa629f

Nasal Dilator Patch (Unsterilized)

TW: 鼻舒樂 鼻腔擴張貼片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·Lianya Biotechnology Development Co., Ltd. Hsinchu Factory·Registered Jan 14, 2010 – Jan 14, 2015Cancelled
Registration details
Analysis ID
609eca6f3abd5011e2488a06d9fa629f
Company information
Manufacturer Country
Taiwan, Province of China
Product details
Intended Use
Limited to the first level recognition range of the "nasal expander (G.3900)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1)
G ENT Science
Product Type (Level 2)
G.3900 Nasal extenders
Import Information
Domestic;; Contract manufacturing
Dates and status
Registration Date
Jan 14, 2010
Expiry Date
Jan 14, 2015
Cancellation Date
Jun 28, 2018
Cancellation information
Status
Logged out
Reason
許可證已逾有效期
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About this record

Access comprehensive regulatory information for Nasal Dilator Patch (Unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 609eca6f3abd5011e2488a06d9fa629f and manufactured by Lianya Biotechnology Development Co., Ltd. Hsinchu Factory. The authorized representative in Taiwan is GLAXOSMITHKLINE FAR EAST B.V., TAIWAN BRANCH (NETHERLANDS).

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including WEBTEC CONVERTING LLC, Somnifix International LLC, and 4 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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