Taiwan FDA registration 2c5760a57f0330f70e43711e475ebc5c

"C-PRO DIRECT" Limb orthosis (Non-Sterile)

TW: "希柏德瑞特" 肢體裝具 (未滅菌)

Taiwan·Risk Class 1·MD·C-Pro Direct Ltd.·Registered Feb 16, 2016 – Feb 16, 2021Expired

Registration details

Analysis ID: 2c5760a57f0330f70e43711e475ebc5c
License Form: Ministry of Health Medical Device Import No. 016160
Customs Code: DHA09401616005

Company information

Manufacturer: C-Pro Direct Ltd.
Manufacturer Country: United Kingdom
Authorized Representative: INNOVATIVE HEALTHCARE LTD.

Product details

Intended Use: Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.
Product Type (Level 1): o Equipment for physical medicine
Product Type (Level 2): O3475 Body Equipment
Import Information: Imported from abroad

Dates and status

Registration Date: Feb 16, 2016
Expiry Date: Feb 16, 2021

About this record

Access comprehensive regulatory information for "C-PRO DIRECT" Limb orthosis (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 2c5760a57f0330f70e43711e475ebc5c and manufactured by C-Pro Direct Ltd.. The authorized representative in Taiwan is INNOVATIVE HEALTHCARE LTD..

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