Taiwan FDA registration d17bf15a55058f2a552d369fb17319ae
“KIYOKAWA”Limb orthosis (Non-Sterile)
TW: “奇優克瓦”肢體裝具 (未滅菌)
Taiwan·Risk Class 1·MD·KIYOKAWA CO., LTD.·Registered Oct 01, 2021 – Oct 31, 2023ExpiredRegistration details
- Analysis ID
- d17bf15a55058f2a552d369fb17319ae
- License Form
- Ministry of Health Medical Device Import Registration No. 006882
- Customs Code
- DHA08400688202
Company information
- Manufacturer
- KIYOKAWA CO., LTD.
- Manufacturer Country
- Japan
- Authorized Representative
- PURIGO BIOTECH INC.
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
- Oct 01, 2021
- Expiry Date
- Oct 31, 2023
About this record
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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