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"TRIO" Genii Flang Extender (Non-Sterile) - Taiwan Registration ae6524b368f2e0f1f5e6b91c87ee85ff

Access comprehensive regulatory information for "TRIO" Genii Flang Extender (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 ae6524b368f2e0f1f5e6b91c87ee85ff and manufactured by TRIO HEALTHCARE LTD.. The authorized representative in Taiwan is MIMED CO., LTD..

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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ae6524b368f2e0f1f5e6b91c87ee85ff
Registration Details
Taiwan FDA Registration: ae6524b368f2e0f1f5e6b91c87ee85ff
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Device Details

"TRIO" Genii Flang Extender (Non-Sterile)
TW: "็‰น็ซ‹ๅ„ช"ๆฝ”ๅฏง็Ÿฝ่† ๅŠ ๅ›บ็’ฐ (ๆœชๆป…่Œ)
Risk Class 1
MD

Registration Details

ae6524b368f2e0f1f5e6b91c87ee85ff

Ministry of Health Medical Device Import No. 022802

DHA09402280205

Company Information

United Kingdom

Product Details

Limited to the first level identification range of the "ostomy bag and its accessories (H.5900)" of the Measures for the Classification and Grading Management of Medical Equipment.

H Gastroenterology and urology

H5900 Ostomy bag and accessories

Imported from abroad

Dates and Status

May 11, 2022

May 11, 2027