Taiwan FDA registration d950792203d67b185fdc0dc4cec693aa
“Alcare” Limb Orthosis(Non-Sterile)
TW: “愛樂康”肢體裝具（未滅菌）
Taiwan·Risk Class 1·MD·ALCARE CO., LTD., CHIBA FACTORY WEST·Registered Oct 01, 2021 – Oct 31, 2025ExpiredRegistration details
- Analysis ID
- d950792203d67b185fdc0dc4cec693aa
- License Form
- Ministry of Health Medical Device Import Registration No. 008862
- Customs Code
- DHA08400886206
Company information
- Manufacturer
- ALCARE CO., LTD., CHIBA FACTORY WEST
- Manufacturer Country
- Japan
- Authorized Representative
- HORIZON INSTRUMENTS 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
- Imported from abroad
Dates and status
- Registration Date
- Oct 01, 2021
- Expiry Date
- Oct 31, 2025
About this record
Access comprehensive regulatory information for “Alcare” 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 d950792203d67b185fdc0dc4cec693aa and manufactured by ALCARE CO., LTD., CHIBA FACTORY WEST. The authorized representative in Taiwan is HORIZON INSTRUMENTS CO. ,LTD..
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