Taiwan FDA registration 171e5ead1d51daf0993f71da9b277833

Nasal Dilator Patch (Unsterilized)

TW: 鼻舒樂 鼻腔擴張貼片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·WEBTEC CONVERTING LLC·Registered Jul 15, 2008 – Jul 15, 2018Cancelled
Registration details
Analysis ID
171e5ead1d51daf0993f71da9b277833
Customs Code
DHA04400691201
Company information
Manufacturer Country
United States
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
import
Dates and status
Registration Date
Jul 15, 2008
Expiry Date
Jul 15, 2018
Cancellation Date
Jun 07, 2022
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 171e5ead1d51daf0993f71da9b277833 and manufactured by WEBTEC CONVERTING LLC. The authorized representative in Taiwan is HALEON UK SERVICES LIMITED TAIWAN BRANCH.

This page provides complete technical specifications, regulatory compliance details, 4 companies making similar products including Lianya Biotechnology Development Co., Ltd. Hsinchu Factory, 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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