Taiwan FDA registration 2cd7d2de3ce47d87eaa15657e77032f4

"Hongang" in vitro assembly of lower limb prosthesis (unsterilized)

TW: “宏昂”體外組裝下肢義肢(未滅菌)

Taiwan·Risk Class 1·HURN ARNG ENTERPRISE CO., LTD.·Registered Apr 30, 2014 – Apr 30, 2024Expired

Registration details

Analysis ID: 2cd7d2de3ce47d87eaa15657e77032f4

Company information

Manufacturer: HURN ARNG ENTERPRISE CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: HURN ARNG ENTERPRISE CO., LTD.

Product details

Intended Use: Limited to the classification and grading management method of medical equipment, in vitro assembly of lower limb prosthetics (O.3500) first level recognition range.
Product Type (Level 1): o Physical Medical Sciences
Product Type (Level 2): O.3500 shades
Import Information: Domestic

Dates and status

Registration Date: Apr 30, 2014
Expiry Date: Apr 30, 2024

About this record

Access comprehensive regulatory information for "Hongang" in vitro assembly of lower limb prosthesis (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number 2cd7d2de3ce47d87eaa15657e77032f4 and manufactured by HURN ARNG ENTERPRISE CO., LTD.. The authorized representative in Taiwan is HURN ARNG ENTERPRISE CO., LTD..

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