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“KIYOKAWA”Limb orthosis (Non-Sterile)  - Taiwan Registration d17bf15a55058f2a552d369fb17319ae

Access comprehensive regulatory information for “KIYOKAWA”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 d17bf15a55058f2a552d369fb17319ae and manufactured by KIYOKAWA CO., LTD.. The authorized representative in Taiwan is PURIGO BIOTECH INC..

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d17bf15a55058f2a552d369fb17319ae
Registration Details
Taiwan FDA Registration: d17bf15a55058f2a552d369fb17319ae
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Device Details

“KIYOKAWA”Limb orthosis (Non-Sterile) 
TW: “奇優克瓦”肢體裝具 (未滅菌)
Risk Class 1
MD

Registration Details

d17bf15a55058f2a552d369fb17319ae

Ministry of Health Medical Device Import Registration No. 006882

DHA08400688202

Company Information

Japan

Product Details

Limited to the first level recognition range of limb equipment (O.3475) of the Measures for the Administration of Medical Devices.

o Equipment for physical medicine

O3475 Body Equipment

Imported from abroad

Dates and Status

Oct 01, 2021

Oct 31, 2023