Taiwan FDA registration 5fb0f6555a7c3240bb1cb35c601314d1

"CLEARSCOPE" Surgical camera and accessories (Non-Sterile)

TW: "可力而視"外科手術用照相機及其附件 (未滅菌)

Taiwan·Risk Class 1·MD·CLEARWATER CLINICAL LIMITED·Registered Oct 20, 2017 – Oct 20, 2022Expired

Registration details

Analysis ID: 5fb0f6555a7c3240bb1cb35c601314d1
License Form: Ministry of Health Medical Device Import No. 018436
Customs Code: DHA09401843604

Company information

Manufacturer: CLEARWATER CLINICAL LIMITED
Manufacturer Country: Canada
Authorized Representative: GOLDENSPRING MEDI-TECH CO., LTD.

Product details

Intended Use: Limited to the first level of identification scope of the Measures for the Administration of Medical Devices "Surgical Cameras and Their Accessories (I.4160)".
Product Type (Level 1): I General and plastic surgical devices
Product Type (Level 2): I4160 Surgical Camera and Its Accessories
Import Information: Imported from abroad

Dates and status

Registration Date: Oct 20, 2017
Expiry Date: Oct 20, 2022

About this record

Access comprehensive regulatory information for "CLEARSCOPE" Surgical camera and accessories (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 5fb0f6555a7c3240bb1cb35c601314d1 and manufactured by CLEARWATER CLINICAL LIMITED. The authorized representative in Taiwan is GOLDENSPRING MEDI-TECH CO., LTD..

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