Taiwan FDA registration 4f09bfda3f58ddc5f6ae19d65fc79d59

"REDA" Rectal dilator (Non-Sterile)

TW: "鐳鐽" 直腸擴張器(未滅菌)

Taiwan·Risk Class 1·MD·REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD·Registered Apr 09, 2021 – Apr 09, 2026Expired

Registration details

Analysis ID: 4f09bfda3f58ddc5f6ae19d65fc79d59
License Form: Ministry of Health Medical Device Import No. 022463
Customs Code: DHA09402246309

Company information

Manufacturer: REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD
Manufacturer Country: Singapore
Authorized Representative: Medical Dragon Ltd.

Product details

Intended Use: Limited to the first level identification range of "rectal dilator (H.5450)" of the Measures for the Administration of Medical Devices.
Product Type (Level 1): H Gastroenterology-urology devices
Product Type (Level 2): H5450 Rectal dilators
Import Information: Imported from abroad

Dates and status

Registration Date: Apr 09, 2021
Expiry Date: Apr 09, 2026

About this record

Access comprehensive regulatory information for "REDA" Rectal dilator (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 4f09bfda3f58ddc5f6ae19d65fc79d59 and manufactured by REDA INSTRUMENTE (ASIA -PACIFIC) PTE LTD. The authorized representative in Taiwan is Medical Dragon Ltd..

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