Taiwan FDA registration eb1afead81061484c358f4bfb9436c94

"BONEMETAL" LIMB ORTHOSIS (Non-Sterile)

TW: "溋溢" 肢體裝具 (未滅菌)

Taiwan·Risk Class 1·MD·BONE METAL CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2026Active

Registration details

Analysis ID: eb1afead81061484c358f4bfb9436c94
License Form: Ministry of Health Medical Device Manufacturing Registration No. 006151

Company information

Manufacturer: BONE METAL CO., LTD.
Manufacturer Country: Taiwan, Province of China
Authorized Representative: BONE METAL CO., 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: Produced in Taiwan, China

Dates and status

Registration Date: Oct 01, 2021
Expiry Date: Oct 31, 2026

About this record

Access comprehensive regulatory information for "BONEMETAL" 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 eb1afead81061484c358f4bfb9436c94 and manufactured by BONE METAL CO., LTD.. The authorized representative in Taiwan is BONE METAL CO., LTD..

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