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"Sophie Sliri" nasal dilator patch (unsterilized) - Taiwan Registration ae752533dd58532dc55c4041e79b2f62

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..

This page provides complete technical specifications, regulatory compliance details. 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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ae752533dd58532dc55c4041e79b2f62
Registration Details
Taiwan FDA Registration: ae752533dd58532dc55c4041e79b2f62
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Device Details

"Sophie Sliri" nasal dilator patch (unsterilized)
TW: โ€œ็ดข้ฃ›ๅฒๅˆฉ็‘žโ€้ผป่…”ๆ“ดๅผต่ฒผ็‰‡ (ๆœชๆป…่Œ)
Risk Class 1

Registration Details

ae752533dd58532dc55c4041e79b2f62

DHA09401979501

Company Information

United States

Product Details

Limited to the first level identification range of the "nasal expander (G.3900)" of the classification and grading management method for medical devices.

G ENT Science

G.3900 Nasal extenders

import

Dates and Status

Nov 07, 2018

Nov 07, 2023