Taiwan FDA registration 71c9a919c0fa777c10d8b8a4bc5428d4
"Matsumotokiyoshi" Nasal Dilator (Non-Sterile)
TW: “松本清”鼻腔擴張貼片 (未滅菌)
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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