Taiwan FDA registration f63bc49803e0950ed7b30902de0f13d9

"Miabi" surgical retractor (unsterilized)

TW: “米雅比”手術用牽開器 (未滅菌)

Taiwan·Risk Class 1·MIYABI INTERNATIONAL INC.·Registered Jul 28, 2006 – Jul 28, 2026Expired

Registration details

Analysis ID: f63bc49803e0950ed7b30902de0f13d9
Customs Code: DHA04400498709

Company information

Manufacturer: MIYABI INTERNATIONAL INC.
Manufacturer Country: Japan
Authorized Representative: BARRY TEC ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the "Manual Instruments for General Surgery (I.4800)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): I General, Plastic Surgery and Dermatology
Product Type (Level 2): I.4800 Hand Instruments for General Surgery
Import Information: import

Dates and status

Registration Date: Jul 28, 2006
Expiry Date: Jul 28, 2026

About this record

Access comprehensive regulatory information for "Miabi" surgical retractor (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f63bc49803e0950ed7b30902de0f13d9 and manufactured by MIYABI INTERNATIONAL INC.. The authorized representative in Taiwan is BARRY TEC ENTERPRISE CO., LTD..

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