Taiwan FDA registration e61dc7e58a227e2606e543fe97ab5d48
"Glesine" nasal dilator patch (unsterilized)
TW: “格來素” 鼻腔擴張貼片 (未滅菌)
Taiwan·Risk Class 1·GLAXOSMITHKLINE CO., LTD.·Registered Jan 31, 2011 – Jan 31, 2016CancelledRegistration details
- Analysis ID
- e61dc7e58a227e2606e543fe97ab5d48
- Customs Code
- DHA04400988309
Company information
- Manufacturer
- GLAXOSMITHKLINE CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- Nichimi Pharmaceutical Co., Ltd
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
- Jan 31, 2011
- Expiry Date
- Jan 31, 2016
- Cancellation Date
- Nov 07, 2017
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Glesine" 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 e61dc7e58a227e2606e543fe97ab5d48 and manufactured by GLAXOSMITHKLINE CO., LTD.. The authorized representative in Taiwan is Nichimi Pharmaceutical Co., Ltd.
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