Taiwan FDA registration ae6524b368f2e0f1f5e6b91c87ee85ff

"TRIO" Genii Flang Extender (Non-Sterile)

TW: "特立優"潔寧矽膠加固環 (未滅菌)

Taiwan·Risk Class 1·MD·TRIO HEALTHCARE LTD.·Registered May 11, 2022 – May 11, 2027Active

Registration details

Analysis ID: ae6524b368f2e0f1f5e6b91c87ee85ff
License Form: Ministry of Health Medical Device Import No. 022802
Customs Code: DHA09402280205

Company information

Manufacturer: TRIO HEALTHCARE LTD.
Manufacturer Country: United Kingdom
Authorized Representative: MIMED CO., LTD.

Product details

Intended Use: 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.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H5900 Ostomy bag and accessories
Import Information: Imported from abroad

Dates and status

Registration Date: May 11, 2022
Expiry Date: May 11, 2027

About this record

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..

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