Taiwan FDA registration 0ff55477c314a3e766a187c848d841ce

"De Soutter" Cast removal instrument (Non-sterile)

TW: "迪思坦" 石膏拆除器械 (未滅菌)

Taiwan·Risk Class 1·MD·DE SOUTTER MEDICAL LTD·Registered Aug 16, 2019 – Aug 16, 2024Expired

Registration details

Analysis ID: 0ff55477c314a3e766a187c848d841ce
License Form: Ministry of Health Medical Device Import No. 020763
Customs Code: DHA09402076301

Company information

Manufacturer: DE SOUTTER MEDICAL LTD
Manufacturer Country: United Kingdom
Authorized Representative: YOUR TEAM INTERNATIONAL CO., LTD.

Product details

Intended Use: Limited to the first level identification scope of the Measures for the Administration of Medical Equipment "Gypsum Removal Devices (N.5960)".
Product Type (Level 1): N Orthopedic devices
Product Type (Level 2): N5960 Gypsum removal apparatus
Import Information: Imported from abroad

Dates and status

Registration Date: Aug 16, 2019
Expiry Date: Aug 16, 2024

About this record

Access comprehensive regulatory information for "De Soutter" Cast removal instrument (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 0ff55477c314a3e766a187c848d841ce and manufactured by DE SOUTTER MEDICAL LTD. The authorized representative in Taiwan is YOUR TEAM INTERNATIONAL CO., LTD..

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