Taiwan FDA registration f6c0c7e2506f2559271303ad6dc38694

"Rofo" endoscope attachment (unsterilized)

TW: “羅福”內視鏡附件(未滅菌)

Taiwan·Risk Class 1·THE RUHOF CORPORATION·Registered Dec 04, 2018 – Dec 04, 2028Active

Registration details

Analysis ID: f6c0c7e2506f2559271303ad6dc38694
Customs Code: DHA09401987407

Company information

Manufacturer: THE RUHOF CORPORATION
Manufacturer Country: United States
Authorized Representative: HONYOU DEVELOPMENT CO., LTD.

Product details

Intended Use: Limited to the first level recognition range of the "endoscope and its accessories (H.1500)" of the Measures for the Classification and Grading Management of Medical Equipment.
Product Type (Level 1): H Gastroenterology and urology
Product Type (Level 2): H.1500 Internal Scope and its accessories
Import Information: Input;; QMS/QSD

Dates and status

Registration Date: Dec 04, 2018
Expiry Date: Dec 04, 2028

About this record

Access comprehensive regulatory information for "Rofo" endoscope attachment (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number f6c0c7e2506f2559271303ad6dc38694 and manufactured by THE RUHOF CORPORATION. The authorized representative in Taiwan is HONYOU DEVELOPMENT CO., LTD..

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