Taiwan FDA registration 8b3134bce72571592b8c388b19560782

"Plooz" endoscope cleaning brush (unsterilized)

TW: “撲朔” 內視鏡清潔刷 (未滅菌)

Taiwan·Risk Class 1·F. R. GALANTAI MANUFACTURING COMPANY LIMITED·Registered Aug 06, 2020 – Aug 06, 2025Expired

Registration details

Analysis ID: 8b3134bce72571592b8c388b19560782
Customs Code: DHA09402183400

Company information

Manufacturer: F. R. GALANTAI MANUFACTURING COMPANY LIMITED
Manufacturer Country: New Zealand
Authorized Representative: RECHI 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: Aug 06, 2020
Expiry Date: Aug 06, 2025

About this record

Access comprehensive regulatory information for "Plooz" endoscope cleaning brush (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 8b3134bce72571592b8c388b19560782 and manufactured by F. R. GALANTAI MANUFACTURING COMPANY LIMITED. The authorized representative in Taiwan is RECHI CO., LTD..

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