Taiwan FDA registration 71c9a919c0fa777c10d8b8a4bc5428d4

"Matsumotokiyoshi" Nasal Dilator (Non-Sterile)

TW: “松本清”鼻腔擴張貼片 (未滅菌)
Taiwan flagTaiwan·Risk Class 1·MD·C&TECH CORPORATION·Registered Mar 09, 2020 – Mar 09, 2025Expired
Registration details
Analysis ID
71c9a919c0fa777c10d8b8a4bc5428d4
License Form
Ministry of Health Medical Device Import No. 021351
Customs Code
DHA09402135106
Company information
Manufacturer
C&TECH CORPORATION
Manufacturer Country
Korea, Republic of
Authorized Representative
Matsumotokiyoshi (Taiwan) Limited
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 device
Product Type (Level 2)
G3900 Nasal Enlarger
Import Information
Imported from abroad
Dates and status
Registration Date
Mar 09, 2020
Expiry Date
Mar 09, 2025
About this record

Access comprehensive regulatory information for "Matsumotokiyoshi" Nasal Dilator (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 71c9a919c0fa777c10d8b8a4bc5428d4 and manufactured by C&TECH CORPORATION. The authorized representative in Taiwan is Matsumotokiyoshi (Taiwan) Limited.

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