Taiwan FDA registration ae752533dd58532dc55c4041e79b2f62

"Sophie Sliri" nasal dilator patch (unsterilized)

TW: “索飛史利瑞”鼻腔擴張貼片 (未滅菌)

Taiwan·Risk Class 1·Somnifix International LLC·Registered Nov 07, 2018 – Nov 07, 2023Expired

Registration details

Analysis ID: ae752533dd58532dc55c4041e79b2f62
Customs Code: DHA09401979501

Company information

Manufacturer: Somnifix International LLC
Manufacturer Country: United States
Authorized Representative: BROJAW INC.

Product details

Intended Use: Limited to the first level identification range of the "nasal expander (G.3900)" of the classification and grading management method for 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: Nov 07, 2018
Expiry Date: Nov 07, 2023

About this record

Access comprehensive regulatory information for "Sophie Sliri" 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 ae752533dd58532dc55c4041e79b2f62 and manufactured by Somnifix International LLC. The authorized representative in Taiwan is BROJAW INC..

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